Misuse of Drugs Act 1975 No 116 (as at 08 September 2011), Public Act

Reprint
as at 8 September 2011

Coat of Arms of New Zealand

Misuse of Drugs Act 1975

Public Act1975 No 116
Date of assent10 October 1975
Commencementsee section 1(2)

Note

Changes authorised by section 17C of the Acts and Regulations Publication Act 1989 have been made in this reprint.

A general outline of these changes is set out in the notes at the end of this reprint, together with other explanatory material about this reprint.

This Act is administered by the Ministry of Health.


Contents

Title

1 Short Title and commencement

2 Interpretation

3 Act to bind the Crown

3A Classification of drugs

4 Amendment of schedules that identify controlled drugs and precursor substances, and set amount, level, or quantity at and over which controlled drugs are presumed to be for supply

4A Procedure for bringing Order in Council made under section 4(1) or (1B) into force

4B Matters to which Minister must have regard before recommending Order in Council under section 4(1) or (1B)

4C Temporary class drug notice

4D Effect of temporary class drug notice

4E Duration of temporary class drug notice

5 Advisory and technical committees

5AA Expert Advisory Committee on Drugs

5A Approved laboratories

5B Functions of Minister

6 Dealing with controlled drugs

7 Possession and use of controlled drugs

8 Exemptions from sections 6 and 7

9 Cultivation of prohibited plants

10 Aiding offences against corresponding law of another country

11 Theft, etc, of controlled drugs

12 Use of premises or vehicle, etc

12A Equipment, material, and substances used in production or cultivation of controlled drugs

12AB Offence to knowingly import or export precursor substances for unlawful use

12AC Offence to import or export precursor substance without reasonable excuse

12B Laundering proceeds of drug offences

12C Commission of offences outside New Zealand

13 Miscellaneous offences

14 Licences

15 False statements

16 Obstruction of officers

17 Liability of principal for acts of agent, etc

18 Search and seizure

18A Internal search of person under arrest

19 Power to demand production of records and to inspect stocks of controlled drugs

20 Statements regarding drug dependent persons

21 Power of court to restrict publication of name of controlled drug

22 Powers of Minister to prohibit importation, etc, of controlled drugs

23 Powers of Minister to prohibit prescribing, etc

24 Treatment of people dependent on controlled drugs

25 Restrictions on supply to particular persons

26 Arrest by Customs officers

27 General penalty

28 Legal proceedings

28A Consent of Attorney-General required in proceedings under section 12C

29 Mistake as to nature of controlled drug or precursor substance

29A Issue of usable quantity

29B Special provisions where offence relating to cannabis preparations alleged

29C Special provisions where offence relating to controlled drug analogues alleged

30 Burden of proof

31 Evidence of analysis

32 Forfeiture

33 Notification of conviction of medical practitioners, etc

34 Protection of persons acting under authority of Act

34A Protection of constables

35 Crimes deemed to be included in extradition treaties

35A Further provision on crimes to be treated as included in extradition treaties

35B Surrender of offenders [Repealed]

35C Restrictions on surrender of offenders

35D Evidence

36 Application of Customs and Excise Act 1996

37 Regulations

38 Effect on Poisons Act 1960 [Repealed]

39 Repeals

40 Revocations

41 Application to Niue

Schedule 1
Class A controlled drugs

Schedule 2
Class B controlled drugs

Schedule 3
Class C controlled drugs

Schedule 4
Precursor substances

Schedule 5
Amount, level, or quantity at and over which controlled drugs are presumed to be for supply


An Act to consolidate and amend the Narcotics Act 1965 and to make further provision for the prevention of misuse of drugs

1 Short Title and commencement
  • (1) This Act may be cited as the Misuse of Drugs Act 1975.

    (2) This Act shall come into force on a date to be appointed for the commencement thereof by the Governor-General by Order in Council.

    Section 1(2): Misuse of Drugs Act 1975 brought into force, on 1 June 1977, by the Misuse of Drugs Act Commencement Order 1977 (SR 1977/36).

2 Interpretation
  • (1) In this Act, unless the context otherwise requires,—

    approved laboratory means a laboratory for the time being approved under section 5A

    carrier includes every person engaged in carrying goods (including mail) for hire or reward by any means, and whether by land, water, or air

    Class A controlled drug means the controlled drugs specified or described in Schedule 1

    Class B controlled drug means the controlled drugs specified or described in Schedule 2

    Class C controlled drug means the controlled drugs specified or described in Schedule 3; and includes any controlled drug analogue

    controlled drug means any substance, preparation, mixture, or article specified or described in Schedule 1, Schedule 2, or Schedule 3; and includes any controlled drug analogue

    controlled drug analogue means any substance, such as the substances specified or described in Part 7 of Schedule 3, that has a structure substantially similar to that of any controlled drug; but does not include—

    • (b) any pharmacy-only medicine or prescription medicine or restricted medicine within the meaning of the Medicines Act 1981

    cultivate includes sow or plant; and cultivation has a corresponding meaning

    dentist means a health practitioner who is, or is deemed to be, registered with the Dental Council established by section 114(2) of the Health Practitioners Competence Assurance Act 2003 as a practitioner of the profession of dentistry

    dependent means being in a state of periodic or chronic intoxication, produced by the repeated consumption, smoking, or other use of a controlled drug detrimental to the person in relation to whom the word is used, and involving a compulsive desire to continue consuming, smoking, or otherwise using the drug or a tendency to increase the dose of the drug; and dependency has a corresponding meaning

    designated prescriber has the same meaning as it has in section 2(1) of the Medicines Act 1981

    Medical Officer of Health means a Medical Officer of Health within the meaning of the Health Act 1956; and includes the officers referred to in section 22 of that Act

    medical practitioner means a health practitioner who is, or is deemed to be, registered with the Medical Council of New Zealand continued by section 114(1)(a) of the Health Practitioners Competence Assurance Act 2003 as a practitioner of the profession of medicine

    midwife means a health practitioner who is, or is deemed to be, registered with the Midwifery Council established by section 114(3) of the Health Practitioners Competence Assurance Act 2003 as a practitioner of the profession of midwifery

    Minister means the Minister of Health

    pharmacist means a health practitioner who is, or is deemed to be, registered with the Pharmacy Council established by section 114(5) of the Health Practitioners Competence Assurance Act 2003 as a practitioner of the profession of pharmacy

    precursor substance means any substance specified or described in Part 1 or Part 2 or Part 3 of Schedule 4

    produce includes compound; and production has a corresponding meaning

    prohibited plant means—

    • (a) any plant of the genus Cannabis:

    • (b) any plant of the species Papaver somniferum:

    • (c) Erythroxylon coca and Erythroxylon novagranatense (syn E truxillense) and every other species of the genus Erythroxylon from which a controlled drug can be produced:

    • (d) any plant of the species Lophophora williamsii or Lophophora lewinii:

    • (e) any fungus of the genera Conocybe, Panaeolus, or Psilocybe from which a controlled drug can be produced or which contains a controlled drug:

    • (f) any other plant which is declared to be a prohibited plant by regulations made under this Act

    registered health professional means a health practitioner who is, or is deemed to be, registered with an authority established or continued by section 114 of the Health Practitioners Competence Assurance Act 2003 as a practitioner of a particular health profession

    standing order has the same meaning as it has in section 2(1) of the Medicines Act 1981

    supply includes distribute, give, and sell

    temporary class drug means a substance, preparation, mixture, or article specified in a temporary class drug notice

    temporary class drug notice means a notice given under section 4C

    veterinarian means a veterinarian or a specialist within the meaning of section 4 of the Veterinarians Act 2005

    Vienna Convention means the United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances adopted in Vienna on 19 December 1988.

    (1A) Any reference in this Act to an amount, level, or quantity at and over which a controlled drug is presumed to be for supply is a reference to the amount, level, or quantity specified in Schedule 5.

    (2) For the purposes of this Act, the things which a person has in his possession include any thing subject to his control which is in the custody of another.

    (3) In calculating for the purposes of this Act the percentage of any substance present in a preparation, the percentage in the case of a liquid preparation shall, unless otherwise prescribed, be calculated on the basis that a preparation containing 1 part percent of any substance means a preparation in which 1 gram of the substance, if a solid, or 1 millilitre of the substance, if a liquid, is contained in every 100 millilitres of the preparation and so in proportion for any greater or less percentage.

    (4) In calculating for the purposes of this Act the percentage of morphine present in a preparation it shall be calculated as in respect of anhydrous morphine.

    (5) For the purposes of this Act, a salt of any controlled drug shall be deemed to contain that drug.

    Compare: 1965 No 45 s 2; SR 1966/82 rr 2, 2A, 15(1), 25A(1); SR 1967/173 r 2; SR 1973/100 r 7; Misuse of Drugs Act 1971 s 37(3) (UK)

    Section 2(1) approved laboratory: inserted, on 1 July 1992, by section 2 of the Misuse of Drugs Amendment Act 1992 (1992 No 49).

    Section 2(1) carrier: amended, on 1 April 1998, by section 62(1) of the Postal Services Act 1998 (1998 No 2).

    Section 2(1) Class A controlled drug: inserted, on 2 September 1996, by section 2(2) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Section 2(1) Class B controlled drug: inserted, on 2 September 1996, by section 2(2) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Section 2(1) Class C controlled drug: inserted, on 2 September 1996, by section 2(2) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Section 2(1) controlled drug: substituted, on 2 September 1996, by section 2(1) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Section 2(1) controlled drug analogue: inserted, on 13 January 1988, by section 2(1) of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Section 2(1) dentist: substituted, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 2(1) designated prescriber: inserted, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 2(1) medical practitioner: substituted, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 2(1) midwife: inserted, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 2(1) pharmacist: substituted, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 2(1) precursor substance: inserted, on 12 May 1998, by section 2 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 2(1) precursor substance: amended, on 22 June 2005, by section 3(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 2(1) prohibited plant paragraph (e): substituted, on 13 January 1988, by section 2(2) of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Section 2(1) registered health professional: inserted, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 2(1) registered midwife: repealed, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 2(1) standing order: inserted, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 2(1) temporary class drug: inserted, on 9 August 2011, by section 4 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Section 2(1) temporary class drug notice: inserted, on 9 August 2011, by section 4 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Section 2(1) veterinarian: inserted, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 2(1) veterinary surgeon: repealed, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 2(1) Vienna Convention: added, on 12 May 1998, by section 2 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 2(1A): inserted, on 22 June 2005, by section 3(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 2(5): added, on 13 January 1988, by section 2(3) of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

3 Act to bind the Crown
  • (1) Subject to subsection (2), this Act shall bind the Crown.

    (2) The Governor-General may, by Order in Council, exempt any instrument of the Executive Government of New Zealand, either absolutely or to such extent and subject to such conditions as may be specified in the Order in Council, from all or any of the provisions of this Act, and in that event, or to that extent and subject to compliance with any such conditions, this Act, or the provisions of this Act so specified, as the case may require, shall not bind the Crown in right of that instrument.

    Compare: 1965 No 45 s 3

3A Classification of drugs
  • The classification of a drug under this Act is based on the risk of harm the drug poses to individuals, or to society, by its misuse; and accordingly—

    • (a) drugs that pose a very high risk of harm are classified as Class A drugs; and

    • (b) drugs that pose a high risk of harm are classified as Class B drugs; and

    • (c) drugs that pose a moderate risk of harm are classified as Class C drugs.

    Section 3A: inserted, on 15 November 2000, by section 3 of the Misuse of Drugs Amendment Act 2000 (2000 No 47).

4 Amendment of schedules that identify controlled drugs and precursor substances, and set amount, level, or quantity at and over which controlled drugs are presumed to be for supply
  • (1) The Governor-General may, by Order in Council, in accordance with a recommendation of the Minister, amend Schedule 1, Schedule 2, Schedule 3, and Schedule 4, by doing any 1 or more of the following to any 1 or more of those schedules:

    • (a) adding the name or description of any substance, preparation, mixture, or article to a schedule; or

    • (b) removing the name or description of any substance, preparation, mixture, or article from a schedule; or

    • (c) moving the name or description of any substance, preparation, mixture, or article from one schedule, or Part or clause of a schedule, and inserting that name or description in another schedule, or Part or clause of a schedule.

    (1A) An Order in Council may not be made under subsection (1) in relation to a controlled drug if the effect of the Order in Council is—

    (1B) The Governor-General may, by Order in Council, in accordance with a recommendation of the Minister, amend Schedule 5 by doing any of the following:

    • (a) altering the amount, level, or quantity at and over which any controlled drug is presumed to be for supply:

    • (b) adding any substance, preparation, mixture, or article that is to be classified as a controlled drug to clause 1 of Schedule 5 and the amount, level, or quantity at and over which it is presumed to be for supply.

    (1C) An Order in Council may not be made under subsection (1B)(a) in relation to a controlled drug unless the name or description of the controlled drug is, at the same time, being moved from Schedule 1, 2, or 3, or from a Part or clause of Schedule 1, 2, or 3 to another of those schedules, Parts, or clauses.

    (1D) An Order in Council may not be made under subsection (1B)(b) in relation to a substance, preparation, mixture, or article unless its name or description is, at the same time, being added to Schedule 1, 2, or 3.

    (2) An Order in Council made under subsection (1) or subsection (1B) may not come into force except in accordance with a commencement order made under section 4A.

    (3) Sections 5 to 10 of the Regulations (Disallowance) Act 1989 do not apply to any Order in Council made under subsection (1) or subsection (1B).

    (4) The Governor-General may, by Order in Council,—

    • (a) amend the name or description of any substance, preparation, mixture, or article named or described in Schedule 1, Schedule 2, Schedule 3, or Schedule 5, if the amendment is necessary for the purpose of rendering that name or description consistent with international scientific usage:

    • (c) add to, or remove from, Schedule 4 the name or description of any substance included in that schedule, if the amendment is necessary for the purpose of giving effect to any changes to the Annex to the Vienna Convention.

    (5) No Order in Council may be made under paragraph (a) or paragraph (b) of subsection (4) if it has the effect of classifying, changing the classification of, or declassifying any substance, preparation, mixture, or article.

    Section 4: substituted, on 15 November 2000, by section 4 of the Misuse of Drugs Amendment Act 2000 (2000 No 47).

    Section 4 heading: amended, on 22 June 2005, by section 4(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4(1A): inserted, on 22 June 2005, by section 4(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4(1B): inserted, on 22 June 2005, by section 4(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4(1C): inserted, on 22 June 2005, by section 4(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4(1D): inserted, on 22 June 2005, by section 4(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4(2): amended, on 22 June 2005, by section 4(3) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4(3): amended, on 22 June 2005, by section 4(4) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4(4)(a): amended, on 22 June 2005, by section 4(5) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4(4)(b): amended, on 22 June 2005, by section 4(5) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

4A Procedure for bringing Order in Council made under section 4(1) or (1B) into force
  • (1) Subject to subsection (2), the Governor-General may, by Order in Council, make a commencement order bringing any Order in Council made under section 4(1) or (1B) into force.

    (2) The commencement order may be made only after the Order in Council made under section 4(1) or (1B) has been approved by resolution of the House of Representatives.

    (3) A resolution of the House of Representatives approving an Order in Council made under section 4(1) or (1B) may be made at any time after—

    • (a) the date that is 28 days after the date on which notice that the Order in Council has been made is given in the Gazette; or

    • (b) if the Gazette notice is given during the period commencing on 24 December in one year and ending on 15 January in the following year, 15 February of that following year.

    (4) An Order in Council made under section 4(1) or (1B) lapses if—

    • (a) a motion to approve the Order in Council is defeated; or

    • (b) no motion to approve the Order in Council is agreed to within 1 year of its date of making.

    Section 4A: substituted, on 15 November 2000, by section 4 of the Misuse of Drugs Amendment Act 2000 (2000 No 47).

    Section 4A heading: amended, on 22 June 2005, by section 5(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4A(1): amended, on 22 June 2005, by section 5(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4A(2): amended, on 22 June 2005, by section 5(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4A(3): amended, on 22 June 2005, by section 5(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4A(4): amended, on 22 June 2005, by section 5(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

4B Matters to which Minister must have regard before recommending Order in Council under section 4(1) or (1B)
  • (1) Before recommending to the Governor-General that an Order in Council be made under section 4(1), the Minister must, in respect of each substance, preparation, mixture, or article (drug) referred to in the proposed Order in Council,—

    • (a) consult with, and consider any advice given by, the Expert Advisory Committee on Drugs established under section 5AA, about the drug; and

    • (b) have regard to the matters set out in subsection (2).

    (2) The matters that the Minister must have regard to under subsection (1)(b), and on which the Expert Advisory Committee on Drugs must give advice, are—

    • (a) the likelihood or evidence of drug abuse, including such matters as the prevalence of the drug, levels of consumption, drug seizure trends, and the potential appeal to vulnerable populations; and

    • (b) the specific effects of the drug, including pharmacological, psychoactive, and toxicological effects; and

    • (c) the risks, if any, to public health; and

    • (d) the therapeutic value of the drug, if any; and

    • (e) the potential for use of the drug to cause death; and

    • (f) the ability of the drug to create physical or psychological dependence; and

    • (g) the international classification and experience of the drug in other jurisdictions; and

    • (h) any other matters that the Minister considers relevant.

    (3) Before recommending to the Governor-General that an Order in Council be made under section 4(1B), the Minister must, in relation to the amount, level, or quantity at and over which any controlled drug is to be presumed to be for supply in the proposed Order in Council,—

    • (a) consult with, and consider any advice given by, the Expert Advisory Committee on Drugs established under section 5AA, about the amount, level, or quantity at and over which a controlled drug might be presumed to be for supply; and

    • (b) have regard to the matters in subsection (4).

    (4) The matters that the Minister must have regard to under subsection (3)(b), and on which the Expert Advisory Committee on Drugs may give advice, are—

    • (a) the amount of the drug that could reasonably be possessed for personal use, including, without limitation, levels of consumption, the ability of the drug to create physical or psychological dependence, and the specific effects of the drug; and

    • (b) the amount, level, or quantity at and over which the drug is presumed to be for supply in other jurisdictions; and

    • (c) any other matters that the Minister considers relevant.

    Section 4B: inserted, on 15 November 2000, by section 4 of the Misuse of Drugs Amendment Act 2000 (2000 No 47).

    Section 4B heading: amended, on 22 June 2005, by section 6(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4B(2): amended, on 22 June 2005, by section 6(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4B(3): added, on 22 June 2005, by section 6(3) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 4B(4): added, on 22 June 2005, by section 6(3) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

4C Temporary class drug notice
  • (1) The Minister may, by notice in the Gazette, specify any substance, preparation, mixture, or article as a temporary class drug.

    (2) The Minister must not give notice under subsection (1) if the substance, preparation, mixture, or article is a Class A controlled drug, a Class B controlled drug, a Class C controlled drug, a precursor substance, or a restricted substance (as defined in section 31 of the Misuse of Drugs Amendment Act 2005).

    (3) The Minister must not give notice under subsection (1) unless he or she is satisfied that the substance, preparation, mixture, or article that is to be specified in the notice poses, or may pose, a risk of harm to individuals, or to society.

    (4) A notice under subsection (1) may describe the substance, preparation, mixture, or article by any 1 or more of the following:

    • (a) its chemical name, or 1 of its chemical names:

    • (b) its product name:

    • (c) a description of the substance, preparation, mixture, or article, in the form that the Minister considers appropriate for the purposes of the notice.

    (5) A notice under subsection (1) must state the date on which the notice comes into force.

    (6) The date specified under subsection (5) must not be earlier than 7 days after the date of the publication of the notice in the Gazette.

    Section 4C: inserted, on 9 August 2011, by section 5 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

4D Effect of temporary class drug notice
  • (1) Except as provided in this section, a temporary class drug is to be treated, while the temporary class drug notice remains in force, in the same way as if the drug were a controlled drug that is specified or described in Part 1 of Schedule 3.

    (2) A temporary class drug specified or described in a temporary class drug notice is not to be added to any schedule of this Act while the notice is in force.

    (3) Despite section 7(1), it is not an offence for a person, in relation to a temporary class drug, to do either or both of the following while the temporary class drug notice relating to that drug is in force:

    • (a) to possess for his or her own use less than 56 grams in total of any products (including cigarettes), or any drug forms (including flakes, tablets, or capsules), each containing some quantity of that temporary class drug:

    • (b) to use that temporary class drug.

    (4) Possession by a person of 56 grams or more in total of any products (including cigarettes), or any drug forms (including flakes, tablets, or capsules), each containing some quantity of that temporary class drug is to be treated, for the purposes of this Act, as possession by that person of an amount, level, or quantity at and over which a controlled drug that is specified or described in Part 1 of Schedule 3 is presumed to be for supply.

    (5) A substance that has a structure substantially similar to a temporary class drug is not to be treated as a controlled drug analogue by reason only of that similarity.

    (6) While a temporary class drug notice is in force, the Minister must seek advice, as he or she considers appropriate, under section 5 or 5AA, or both, in relation to the temporary class drug and its appropriate classification, if any (including as a precursor substance, or as a restricted substance as defined in section 31 of the Misuse of Drugs Amendment Act 2005), under this Act.

    (7) As soon as possible after the publication of a temporary class drug notice in the Gazette, and while a temporary class drug notice is in force, the Director-General of Health must ensure that the notice, and information about its effects, is available—

    • (a) on the Ministry of Health's Internet site, in an electronic form that is publicly accessible; and

    • (b) in any other way that the Director-General considers appropriate in the circumstances.

    (8) Despite the Regulations (Disallowance) Act 1989, a temporary class drug notice is not to be treated as a regulation for the purposes of the Acts and Regulations Publication Act 1989.

    Section 4D: inserted, on 9 August 2011, by section 5 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

4E Duration of temporary class drug notice
  • (1) A temporary class drug notice expires at the earliest of—

    • (a) the close of the day that is 1 year after the date on which the notice came into force; or

    • (b) the date on which the substance, preparation, mixture, or article is—

      • (i) classified as a Class A controlled drug; or

      • (ii) classified as a Class B controlled drug; or

      • (iii) classified as a Class C controlled drug; or

      • (iv) added to Schedule 4 as a precursor substance; or

      • (v) classified as a restricted substance (as defined in section 31 of the Misuse of Drugs Amendment Act 2005); or

    • (c) its revocation by the Minister by notice in the Gazette.

    (2) A temporary class drug notice may be renewed by the Minister—

    • (a) prior to the date of its expiry as calculated under subsection (1); and

    • (b) on 1 occasion only; and

    • (c) only for the purpose of allowing sufficient time for the Minister to obtain the advice that is to be sought under section 4D(6).

    Section 4E: inserted, on 9 August 2011, by section 5 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

5 Advisory and technical committees
  • (1) The Minister may from time to time appoint such advisory or technical committees as he thinks fit to advise him for any of the purposes of this Act, and may from time to time determine the functions of any such committee.

    (2) There may be paid out of money appropriated by Parliament for the purpose to the members of any committee appointed under this section remuneration by way of fees, salary, or allowances and travelling allowances and expenses in accordance with the Fees and Travelling Allowances Act 1951, and the provisions of that Act shall apply accordingly as if the committee were a statutory board within the meaning of that Act.

    (3) Subject to the provisions of this Act and of any regulations made under this Act, every such committee may regulate its own procedure.

5AA Expert Advisory Committee on Drugs
  • (1) The Minister must establish an Expert Advisory Committee on Drugs to advise the Minister on drug classification matters.

    (2) The functions of the Committee are—

    • (a) to carry out medical and scientific evaluations of controlled drugs, and any other narcotic or psychotropic substances, preparations, mixtures, or articles; and

    • (b) to make recommendations to the Minister about—

      • (i) whether and how controlled drugs or other substances, preparations, mixtures, or articles should be classified; and

      • (ii) the amount, level, or quantity at and over which any substance, preparation, mixture, or article that is a controlled drug (or is proposed to be classified as a controlled drug), and that is to be specified or described in clause 1 of Schedule 5, is to be presumed to be for supply; and

      • (iii) the level at and over which controlled drugs to which clause 2 of Schedule 5 applies are presumed to be for supply; and

    • (c) to increase public awareness of the Committee’s work, by (for instance) the timely release of papers, reports, and recommendations.

    (3) The Committee must comprise—

    • (a) up to 5 people who, between them, have appropriate expertise in—

      • (i) pharmacology:

      • (ii) toxicology:

      • (iii) drug and alcohol treatment:

      • (iv) psychology:

      • (v) community medicine; and

    • (b) up to 3 people employed in the Public Service (as defined in section 27 of the State Sector Act 1988) who between them have appropriate expertise in—

      • (i) public health:

      • (ii) the appropriateness and safety of pharmaceuticals and their availability to the public:

      • (iii) border control; and

    • (c) 1 Police employee; and

    • (ca) 1 employee of the Ministry of Justice who has appropriate expertise in matters relating to the justice system; and

    • (d) 1 person representing the views of consumers of drug treatment services.

    (4) The Minister must appoint 1 member as chairperson of the Committee.

    (5) Subsections (2) and (3) of section 5 apply to the Expert Advisory Committee on Drugs as if it were a committee established under section 5.

    Section 5AA: inserted, on 15 November 2000, by section 5 of the Misuse of Drugs Amendment Act 2000 (2000 No 47).

    Section 5AA(2)(b)(ii): substituted, on 22 June 2005, by section 7(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 5AA(2)(b)(iii): added, on 22 June 2005, by section 7(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 5AA(3)(c): amended, on 1 October 2008, by section 130(1) of the Policing Act 2008 (2008 No 72).

    Section 5AA(3)(ca): inserted, on 22 June 2005, by section 7(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

5A Approved laboratories
  • (1) The Minister may from time to time, by notice in the Gazette, approve any laboratory for the purposes of this Act.

    (2) Any approval by the Minister of a laboratory as an approved laboratory for the purposes of this Act may be given on such terms and conditions as the Minister thinks fit and as are specified in the notice approving that laboratory.

    (3) Any notice given by the Minister in the Gazette for the purposes of subsection (1) shall be deemed to be a regulation for purposes of the Regulations (Disallowance) Act 1989 and the Interpretation Act 1999.

    Section 5A: inserted, on 1 July 1992, by section 3 of the Misuse of Drugs Amendment Act 1992 (1992 No 49).

    Section 5A(3): amended, on 1 November 1999, pursuant to section 38(1) of the Interpretation Act 1999 (1999 No 85).

5B Functions of Minister
  • For the purposes of this Act, the functions of the Minister include the provision and publication of reports, information, and advice concerning the misuse of drugs and the treatment of persons suffering from the misuse of drugs.

    Section 5B: inserted, on 15 November 2000, by section 6 of the Misuse of Drugs Amendment Act 2000 (2000 No 47).

6 Dealing with controlled drugs
  • (1) Except as provided in section 8, or pursuant to a licence under this Act, or as otherwise permitted by regulations made under this Act, no person shall—

    • (a) import into or export from New Zealand any controlled drug, other than a controlled drug specified or described in Part 6 of Schedule 3; or

    • (b) produce or manufacture any controlled drug; or

    • (c) supply or administer, or offer to supply or administer, any Class A controlled drug or Class B controlled drug to any other person, or otherwise deal in any such controlled drug; or

    • (d) supply or administer, or offer to supply or administer, any Class C controlled drug to a person under 18 years of age; or

    • (e) sell, or offer to sell, any Class C controlled drug to a person of or over 18 years of age; or

    • (f) have any controlled drug in his possession for any of the purposes set out in paragraphs (c), (d), or (e).

    (2) Every person who contravenes subsection (1) commits an offence against this Act and is liable on conviction on indictment to—

    • (a) imprisonment for life where a Class A controlled drug was the controlled drug or one of the controlled drugs in relation to which the offence was committed:

    • (b) imprisonment for a term not exceeding 14 years where paragraph (a) does not apply but a Class B controlled drug was the controlled drug or one of the controlled drugs in relation to which the offence was committed:

    • (c) imprisonment for a term not exceeding 8 years in any other case.

    (2A) Every person who conspires with any other person to commit an offence against subsection (1) commits an offence against this Act and is liable on conviction on indictment to imprisonment for a term—

    • (a) not exceeding 14 years where a Class A controlled drug was the controlled drug or one of the controlled drugs in relation to which the offence was committed:

    • (b) not exceeding 10 years where paragraph (a) does not apply but a Class B controlled drug was the controlled drug or one of the controlled drugs in relation to which the offence was committed:

    • (c) not exceeding 7 years in any other case.

    (3) Notwithstanding anything in section 7 of the Summary Proceedings Act 1957, where any person is summarily convicted of an offence against this section relating to a Class C controlled drug, the District Court may sentence him to imprisonment for a term not exceeding 1 year or to a fine not exceeding $1,000.

    (4) Notwithstanding anything in Part 1 or section 39 or section 81 of the Sentencing Act 2002, where any person is convicted of an offence relating to a Class A controlled drug—

    • (a) against paragraph (c) or paragraph (f) of subsection (1); or

    • (b) against paragraph (a) or paragraph (b) of subsection (1) committed in circumstances indicating to the Judge or court an intention to offend against paragraph (c) of that subsection,—

    the Judge or court shall impose a sentence of imprisonment (within the meaning of that Act) unless, having regard to the particular circumstances of the offence or of the offender, including the age of the offender if he is under 20 years of age, the Judge or court is of the opinion that the offender should not be so sentenced.

    (4A) Without limiting anything in subsections (3) and (4) or in Part 1 or section 39 or section 81 of the Sentencing Act 2002, where any person is convicted of an offence relating to a Class A controlled drug or a Class B controlled drug against any of paragraphs (a), (b), (c), and (f) of subsection (1), the Judge or court, if he or it decides to impose a sentence of imprisonment, shall consider whether or not he or it should also impose a fine.

    (5) For the purposes of paragraph (e) of subsection (1), if it is proved that a person has supplied a controlled drug to another person he shall until the contrary is proved be deemed to have sold that controlled drug to that other person.

    (6) For the purposes of subsection (1)(f), a person is presumed until the contrary is proved to be in possession of a controlled drug for any of the purposes in subsection (1)(c), (d), or (e) if he or she is in possession of the controlled drug in an amount, level, or quantity at or over which the controlled drug is presumed to be for supply (see section 2(1A)).

    (7) [Repealed]

    Compare: 1965 No 45 s 5(1)(a), (b), (d), (e), (2), (3), (6)

    Section 6(1)(a): substituted, on 6 November 1986, by section 2 of the Misuse of Drugs Amendment Act 1986 (1986 No 102).

    Section 6(2): substituted, on 16 October 1978, by section 3(1) of the Misuse of Drugs Amendment Act 1978 (1978 No 65).

    Section 6(2A): inserted, on 16 October 1978, by section 4(1) of the Misuse of Drugs Amendment Act 1978 (1978 No 65).

    Section 6(3): substituted, on 13 January 1983, by section 3(1) of the Misuse of Drugs Amendment Act 1982 (1982 No 151).

    Section 6(4): substituted, on 1 October 1985, by section 150(1) of the Criminal Justice Act 1985 (1985 No 120).

    Section 6(4): amended on 30 June 2002, by section 186 of the Sentencing Act 2002 (2002 No 9).

    Section 6(4A): substituted, on 1 October 1985, by section 150(1) of the Criminal Justice Act 1985 (1985 No 120).

    Section 6(4A): amended, on 30 June 2002, by section 186 of the Sentencing Act 2002 (2002 No 9).

    Section 6(6): substituted, on 22 June 2005, by section 8 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 6(7): repealed, on 22 June 2005, by section 8 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

7 Possession and use of controlled drugs
  • (1) Except as provided in section 8, or pursuant to a licence under this Act, or as otherwise permitted by regulations made under this Act, no person shall—

    • (a) procure or have in his possession, or consume, smoke, or otherwise use, any controlled drug; or

    • (b) supply or administer, or offer to supply or administer, any Class C controlled drug to any other person, or otherwise deal in any such controlled drug.

    (2) Subject to subsection (3), but without prejudice to any liability under section 6, every person who contravenes subsection (1) commits an offence against this Act and is liable on conviction—

    • (a) to imprisonment for a term not exceeding 6 months or to a fine not exceeding $1,000 or to both where a Class A controlled drug was the controlled drug or one of the controlled drugs in relation to which the offence was committed:

    • (b) to imprisonment for a term not exceeding 3 months or to a fine not exceeding $500 or to both in any other case:

    provided that, where any person is convicted of an offence against subsection (1) relating only to a Class C controlled drug and is liable to a penalty under paragraph (b), the Judge or District Court Judge shall not impose a custodial sentence (being a sentence under which a person is liable to be detained in a prison within the meaning of the Corrections Act 2004) unless, by reason of the offender’s previous convictions or of any exceptional circumstances relating to the offence or the offender, the Judge or District Court Judge is of the opinion that such a sentence should be imposed.

    (3) In any proceedings for an offence against this section in respect of the possession of a controlled drug, in which it is proved that the defendant had a controlled drug in his possession, it shall be a defence for him to prove—

    • (a) that, knowing or suspecting it to be a controlled drug, he took possession of it for the purpose of preventing another from committing or continuing to commit an offence in connection with that drug and that as soon as possible after taking possession of it he took all reasonable steps to destroy the drug or to deliver it into the possession of a person lawfully entitled to have possession of it; or

    • (b) that, knowing or suspecting it to be a controlled drug, he took possession of it for the purpose of delivering it into the possession of a person lawfully entitled to have possession of it and that as soon as possible after taking possession of it he took all reasonable steps to deliver it into the possession of such a person.

    (4) Nothing in subsection (3) shall prejudice any defence which it is open to a person charged with an offence against this section to raise apart from that subsection.

    Compare: 1965 No 45 s 6; Misuse of Drugs Act 1971 s 5(4), (6) (UK)

    Section 7(2) proviso: amended, on 1 June 2005, by section 206 of the Corrections Act 2004 (2004 No 50).

    Section 7(2) proviso: amended, on 1 April 1980, pursuant to section 18(2) of the District Courts Amendment Act 1979 (1979 No 125).

8 Exemptions from sections 6 and 7
  • (1) In subsection (2), references to a medical practitioner, dentist, veterinarian, midwife, designated prescriber, or pharmacist mean a medical practitioner, dentist, veterinarian, midwife, designated prescriber, or pharmacist, acting as such in the course of his or her practice or employment, and references to the supply of controlled drugs include an offer to supply controlled drugs.

    (2) Notwithstanding anything in section 6 or section 7, but subject to sections 22 to 25 and any prohibitions, limitations, restrictions, or conditions, imposed thereby or thereunder or by or pursuant to any regulations under this Act,—

    • (a) any medical practitioner, dentist or veterinarian may prescribe, produce, manufacture, supply, or administer controlled drugs:

    • (aa) any midwife may prescribe, supply, or administer the controlled drug pethidine (as described in Schedule 2):

    • (b) any pharmacist or any person with the authority and under the immediate supervision of a pharmacist may produce, manufacture, or supply controlled drugs—

      • (ii) for the purposes of the hospital in which he or she is employed; or

      • (iii) pursuant to a prescription or order issued by a medical practitioner, dentist, designated prescriber, or veterinarian:

    • (ba) any pharmacist or any person with the authority and under the immediate supervision of a pharmacist may produce, manufacture, or supply pethidine (as so described) pursuant to a prescription or order issued by a midwife:

    • (c) any person for whom a controlled drug is supplied by a medical practitioner or dentist, or prescribed by a medical practitioner or dentist and lawfully supplied, may administer that drug to himself in accordance with the advice of the medical practitioner or dentist who supplied or prescribed it:

    • (d) any person having the care of a patient for whom a controlled drug is supplied by a medical practitioner or dentist, or prescribed by a medical practitioner or dentist and lawfully supplied, may administer that drug to that patient in accordance with the advice of the medical practitioner or dentist who supplied or prescribed it:

    • (da) any person having the care of a patient for whom pethidine (as so described) is supplied by a midwife, or prescribed by a midwife and lawfully supplied, may administer that drug to that patient in accordance with the advice of the midwife who supplied or prescribed it:

    • (e) any person having the care of an animal for which a controlled drug is supplied by a veterinarian, or prescribed by a veterinarian and lawfully supplied, may administer that drug to that animal in accordance with the advice of the veterinarian who supplied or prescribed it:

    • (f) any district health board established by or under the New Zealand Public Health and Disability Act 2000 or other corporate body, and any individual person being the manager or person licensed to carry on a hospital or any other institution, having the care of patients for whom controlled drugs are lawfully prescribed or supplied, may possess those drugs for the purposes of the treatment of those patients:

    • (g) any person in the service of the Crown or any Medical Officer of Health or any pharmacist approved by a Medical Officer of Health may procure and possess a controlled drug for the purposes of and in connection with his official duties:

    • (h) any carrier may possess a controlled drug in the course of carriage to such extent as is necessary or incidental to his business:

    • (i) any person who is permitted by or under this Act to import, export, supply, or administer a controlled drug may procure that drug from a person lawfully entitled to supply it and may possess that drug in the manner and for the purposes expressed or implied in that authority:

    • (j) any person who is licensed or otherwise permitted under this Act to cultivate a prohibited plant may possess any controlled drug derived from that plant in the manner and for the purposes expressed or implied in that authority:

    • (k) any person who is permitted by or under this Act to possess a controlled drug may procure that drug from a person lawfully entitled to supply it, and may supply or use that drug in the manner and for the purposes expressed or implied in that authority.

    • (l) a person may, while entering or leaving New Zealand, possess a controlled drug required for treating the medical condition of the person or any other person in his or her care or control, if the quantity of drug is no greater than that required for treating the medical condition for 1 month, and the drug was—

      • (i) lawfully supplied to the person by a medical practitioner, designated prescriber (as defined in section 2(1) of the Medicines Act 1981), or dentist in New Zealand; or

      • (ii) prescribed by a medical practitioner, designated prescriber (as defined in section 2(1) of the Medicines Act 1981), or dentist, and lawfully supplied to the person in New Zealand; or

      • (iii) lawfully supplied to the person overseas and supplied for the purpose of treating a medical condition.

    (2A) Despite sections 6 and 7, but subject to sections 22 to 25 and any prohibitions, limitations, restrictions, or conditions imposed under those sections or any regulations made under this Act,—

    • (a) a designated prescriber or any midwife who is authorised by regulations made under this Act to prescribe controlled drugs of any specified class or description, may prescribe, supply, or administer such drugs:

    • (b) a person who is authorised to issue a standing order may include in a standing order authority to supply and administer controlled drugs of any specified class or description, and a person who is authorised under a standing order to supply and administer any controlled drugs may supply and administer those drugs in accordance with that standing order.

    (2B) In subsection (2A),—

    • (a) references to a designated prescriber or a person authorised under a standing order to supply and administer any controlled drugs, mean a designated prescriber or person acting in the course of his or her practice or employment; and

    • (b) references to the supply of controlled drugs include an offer to supply controlled drugs.

    (3) Subject to section 22 and to any regulations under this Act and to any other enactment or rule of law prohibiting, restricting, or regulating the import, export, supply, or administration of drugs, any person may—

    • (a) import or export any controlled drug specified or described in Part 6 of Schedule 3:

    • (b) supply or administer any controlled drug specified or described in the said Part 6.

    Compare: 1965 No 45 s 6(3); SR 1966/82 rr 2(2), 14, 15, 16(1), (a), (b), (e), 17(1), (2)

    Section 8(1): amended, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 8(1): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 8(1): amended, on 22 October 2003, by section 3(1) of the Misuse of Drugs Amendment Act 2003 (2003 No 86).

    Section 8(1): amended, on 28 August 1990, by section 14(1)(a) of the Nurses Amendment Act 1990 (1990 No 107).

    Section 8(1): amended, on 28 August 1990, by section 14(1)(b) of the Nurses Amendment Act 1990 (1990 No 107).

    Section 8(2)(a): amended, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 8(2)(aa): inserted, on 28 August 1990, by section 14(2) of the Nurses Amendment Act 1990 (1990 No 107).

    Section 8(2)(aa): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 8(2)(b): substituted, on 22 October 2003, by section 3(2) of the Misuse of Drugs Amendment Act 2003 (2003 No 86).

    Section 8(2)(b): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 8(2)(ba): inserted, on 28 August 1990, by section 14(3) of the Nurses Amendment Act 1990 (1990 No 107).

    Section 8(2)(ba): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 8(2)(da): inserted, on 28 August 1990, by section 14(4) of the Nurses Amendment Act 1990 (1990 No 107).

    Section 8(2)(da): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 8(2)(e): amended, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 8(2)(f): substituted, on 1 July 1983, by section 32 of the Health Reforms (Transitional Provisions) Act 1993 (1993 No 23).

    Section 8(2)(f): amended, on 1 January 2001, by section 111(1) of the New Zealand Public Health and Disability Act 2000 (2000 No 91).

    Section 8(2)(g): substituted, on 1 July 1993, by section 32 of the Health Reforms (Transitional Provisions) Act 1993 (1993 No 23).

    Section 8(2)(l): added, on 15 November 2000, by section 8 of the Misuse of Drugs Amendment Act 2000 (2000 No 47).

    Section 8(2A): inserted, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 8(2A)(a): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 8(2B): inserted, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 8(3)(a): amended, on 2 September 1996, by section 4 of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

9 Cultivation of prohibited plants
  • (1) Except pursuant to a licence under this Act, or as otherwise permitted by regulations made under this Act, no person shall cultivate any prohibited plant.

    (2) Subject to subsection (4), every person who contravenes subsection (1) commits an offence against this Act and is liable on conviction on indictment to imprisonment for a term not exceeding 7 years.

    (3) Notwithstanding anything in section 7 of the Summary Proceedings Act 1957, where any person is summarily convicted of an offence against this section, the District Court may sentence him to imprisonment for a term not exceeding 2 years or to a fine not exceeding $2,000 or to both.

    (4) It shall be a defence to a charge under subsection (1) if the person charged proves that the prohibited plant to which the charge relates was of the species Papaver somniferum, and that it was not intended to be a source of any controlled drug or that it was not being developed as a strain from which a controlled drug could be produced.

    Compare: 1965 No 45 s 5(1)(c), (2), (5)

    Section 9(3): amended, on 1 April 1980, pursuant to section 18(2) of the District Courts Amendment Act 1979 (1979 No 125).

10 Aiding offences against corresponding law of another country
  • (1) Every person commits an offence against this Act who, in New Zealand, aids, incites, counsels, or procures the doing or omission in any place outside New Zealand of any act, if that act or omission—

    • (a) is punishable under the provisions of any law corresponding to section 6, 9, 12A, or 12AB and in force in that place; or

    • (b) would if done or omitted in New Zealand constitute an offence against section 6, 9, 12A, or 12AB.

    (2) Every person who commits an offence against this section is liable on conviction on indictment to imprisonment for a term—

    • (a) not exceeding 14 years where the relevant act or omission is punishable under the provisions of any law corresponding to section 6 or would if done or omitted in New Zealand constitute an offence against that section:

    • (b) not exceeding 7 years in any other case.

    (3) Notwithstanding anything in section 7 of the Summary Proceedings Act 1957, where any person is summarily convicted of an offence against this section, the District Court may sentence him to imprisonment for a term not exceeding 3 years or to a fine not exceeding $2,000 or to both.

    (4) It is a defence to a charge under paragraph (b) of subsection (1) if the doing or omission of the act to which the charge relates was not an offence under the law of the place where it was, or was to be, done or omitted.

    (5) Nothing in subsection (1) or subsection (4) shall derogate from any provision in the Crimes Act 1961.

    (6) [Repealed]

    Compare: 1965 No 45 s 5A; 1970 No 27 s 3

    Section 10(1)(a): amended, on 22 June 2005, by section 9 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 10(1)(b): amended, on 22 June 2005, by section 9 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 10(3): amended, on 1 April 1980, pursuant to section 18(2) of the District Courts Amendment Act 1979 (1979 No 125).

    Section 10(4): amended, on 12 May 1998, by section 4 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 10(6): repealed, on 1 September 1999, by section 111 of the Extradition Act 1999 (1999 No 55).

11 Theft, etc, of controlled drugs
  • (1) Every person commits an offence against this Act and is liable on conviction on indictment to imprisonment for a term not exceeding 7 years who—

    • (a) steals a controlled drug; or

    • (b) with intent to defraud by any false pretence, either directly or through the medium of any contract obtained by the false pretence, obtains possession of or title to a controlled drug, or procures a controlled drug to be delivered to any person other than himself; or

    • (c) receives a controlled drug obtained by any crime, or by any act, wherever committed, that, if committed in New Zealand, would constitute a crime, knowing that the controlled drug had been dishonestly obtained or being reckless as to whether or not the controlled drug had been stolen or so obtained.

    (2) Section 246(2) to (5) of the Crimes Act 1961 shall apply in respect of any proceedings for an offence against paragraph (c) of subsection (1).

    (3) The definition of crime in section 2, and sections 219, 220, 222, 240, and 246(2) to (5) of the Crimes Act 1961, shall apply, with such modifications as may be necessary, for the purpose of construing subsection (1).

    Compare: 1965 No 45 s 6A; 1970 No 27 s 4(1)

    Section 11(1)(c): substituted, on 1 October 2003, by section 34 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 11(2): amended, on 1 October 2003, by section 34 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 11(3): amended, on 1 October 2003, by section 34 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 11(3): amended, on 1 September 1995, by section 4(3) of the Crimes Amendment Act 1995 (1995 No 49).

12 Use of premises or vehicle, etc
  • (1) Every person commits an offence against this Act who knowingly permits any premises or any vessel, aircraft, hovercraft, motor vehicle, or other mode of conveyance to be used for the purpose of the commission of an offence against this Act.

    (2) Every person who commits an offence against this section is liable on conviction on indictment to imprisonment for a term—

    • (a) not exceeding 10 years where a Class A controlled drug was the controlled drug or one of the controlled drugs in relation to which the offence was committed:

    • (b) not exceeding 7 years where paragraph (a) does not apply but a Class B controlled drug was the controlled drug or one of the controlled drugs in relation to which the offence was committed:

    • (c) not exceeding 3 years in any other case.

    (3) Notwithstanding anything in section 7 of the Summary Proceedings Act 1957, where any person is summarily convicted of an offence against this section the District Court may sentence him—

    • (a) to imprisonment for a term not exceeding 2 years or to a fine not exceeding $1,000 or to both where he could have been sentenced under paragraph (a) of subsection (2) if he had been convicted on indictment:

    • (b) to imprisonment for a term not exceeding 1 year or to a fine not exceeding $1,000 or to both where he could have been sentenced under paragraph (b) of subsection (2) if he had been convicted on indictment:

    • (c) to imprisonment for a term not exceeding 6 months or to a fine not exceeding $500 or to both in any other case.

    Compare: 1965 No 45 s 7(1)(a)

    Section 12 heading: amended, on 16 October 1978, by section 6 of the Misuse of Drugs Amendment Act 1978 (1978 No 65).

    Section 12(1): amended, on 16 October 1978, by section 6 of the Misuse of Drugs Amendment Act 1978 (1978 No 65).

    Section 12(3): amended, on 1 April 1980, pursuant to section 18(2) of the District Courts Amendment Act 1979 (1979 No 125).

12A Equipment, material, and substances used in production or cultivation of controlled drugs
  • (1) Every person commits an offence against this Act who supplies, produces, or manufactures—

    • (a) any equipment or material that is capable of being used in, or for, the commission of an offence against section 6(1)(b) or section 9; or

    • (b) any precursor substance—

    knowing that the equipment, material, or substance is to be used in, or for, the commission of an offence against those provisions.

    (2) Every person commits an offence against this Act who has in his or her possession—

    • (a) any equipment or material that is capable of being used in, or for, the commission of an offence against section 6(1)(b) or section 9; or

    • (b) any precursor substance—

    with the intention that the equipment, material, or substance is to be used in, or for, the commission of an offence against that provision.

    (3) Every person who commits an offence against this section is liable on conviction on indictment,—

    • (a) in the case of an offence against subsection (1), to imprisonment for a term not exceeding 7 years:

    • (b) in the case of an offence against subsection (2), to imprisonment for a term not exceeding 5 years.

    (4) If a person is summarily convicted of an offence against this section,—

    • (a) the court may sentence the person to imprisonment for a term not exceeding 1 year or to a fine not exceeding $1,000, or to both; and

    • (b) the sentencing limits contained in section 7 of the Summary Proceedings Act 1957 do not apply.

    Section 12A: inserted, on 12 May 1998, by section 5 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

12AB Offence to knowingly import or export precursor substances for unlawful use
  • (1) Every person commits an offence who—

    • (a) imports into New Zealand any precursor substance knowing that it will be used to commit an offence under section 6(1)(b) (which is the offence of producing or manufacturing any controlled drug); or

    • (b) exports from New Zealand any precursor substance knowing that it will be used to commit an offence under a provision of the law of the country to which the precursor substance is being exported that corresponds to an offence under section 6(1)(b).

    (2) A person who commits an offence under subsection (1) is liable on conviction on indictment to imprisonment for a term not exceeding 7 years.

    (3) If a person is summarily convicted of an offence under subsection (1),—

    • (a) a court may sentence the person to imprisonment for a term not exceeding 1 year or a fine not exceeding $1,000, or both; and

    • (b) the sentencing limits contained in section 7 of the Summary Proceedings Act 1957 do not apply.

    Section 12AB: inserted, on 22 June 2005, by section 10 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

12AC Offence to import or export precursor substance without reasonable excuse
  • (1) Every person commits an offence who, without reasonable excuse, imports into, or exports from, New Zealand any precursor substance.

    (2) Without limiting the circumstances under subsection (1) in which a person may have a reasonable excuse, a person has a reasonable excuse if—

    • (a) he or she imports a precursor substance into New Zealand in order that—

      • (i) a medical practitioner, dentist, or veterinarian may, in the circumstances referred to in section 8(2)(a), produce or manufacture a controlled drug from the precursor substance; or

      • (ii) a pharmacist or any person with the authority and under the immediate supervision of a pharmacist may, in any of the circumstances referred to in section 8(2)(b), produce or manufacture a controlled drug from the precursor substance; or

      • (iii) the precursor substance be used for a lawful purpose (including, without limitation, an agricultural, commercial, or industrial purpose); or

    • (b) the precursor substance that he or she is importing into, or exporting from, New Zealand has been lawfully supplied to that person for his or her own medical use; or

    • (c) he or she exports a precursor substance from New Zealand in order that the precursor substance be used for a purpose that is authorised or lawful under the law of the country to which it is being exported.

    (3) The requirements in section 67(8) of the Summary Proceedings Act 1957 relating to proof of any exception, excuse, or qualification do not apply to an offence under subsection (1).

    (4) By way of explanation, the effect of subsection (3) is that, in order for a prosecution to be successful, the prosecution must negate beyond a reasonable doubt any reasonable excuse in dispute (being any matter raised as a reasonable excuse by the defendant).

    (5) A person who commits an offence under subsection (1) is liable on summary conviction to imprisonment for a term not exceeding 1 year or a fine not exceeding $1,000, or both.

    Section 12AC: inserted, on 22 June 2005, by section 10 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

12B Laundering proceeds of drug offences
  • (1) In this section,—

    conceal, in relation to property,—

    • (a) means to conceal or disguise the property; and

    • (b) includes (without limitation)—

      • (i) to convert the property from one form to another:

      • (ii) to conceal or disguise the nature, source, location, disposition, or ownership of the property or of any interest in the property

    deal with, in relation to property,—

    • (a) means to deal with the property in any manner and by any means; and

    • (b) includes (without limitation)—

      • (i) to dispose of the property, whether by way of sale, purchase, gift, or otherwise:

      • (ii) to transfer possession of the property:

      • (iii) to bring the property into New Zealand:

      • (iv) to remove property from New Zealand

    interest, in relation to property, means—

    • (a) a legal or equitable estate or interest in the property:

    • (b) a right, power, or privilege in connection with the property

    proceeds, in relation to a specified drug offence, means any property that is derived or realised, directly or indirectly, by any person from the commission of the offence

    property

    • (a) means real or personal property of any description, whether situated in New Zealand or elsewhere and whether tangible or intangible; and

    • (b) includes an interest in any such real or personal property

    serious offence has the same meaning as it has in section 243 of the Crimes Act 1961

    specified drug offence

    • (b) includes any act, wherever committed, which if committed in New Zealand would constitute an offence against any of those sections.

    (2) Subject to subsections (6) to (8), every person commits an offence and is liable on conviction on indictment to imprisonment for a term not exceeding 7 years who, in respect of any property that is the proceeds of a specified drug offence, engages in a money laundering transaction, knowing or believing that all or part of the property is the proceeds of a specified drug offence, or being reckless as to whether or not the property is the proceeds of a specified drug offence.

    (3) Subject to subsections (6) to (8), every person commits an offence and is liable on conviction on indictment to imprisonment for a term not exceeding 5 years who obtains or has in his or her possession any property (which property is the proceeds of a specified drug offence committed by another person)—

    • (a) with intent to engage in a money laundering transaction concerning that property; and

    • (b) knowing or believing that all or part of the property is the proceeds of a specified drug offence, or being reckless as to whether or not the property is the proceeds of a specified drug offence.

    (4) For the purposes of this section, a person engages in a money laundering transaction if that person—

    • (a) deals with any property; or

    • (b) assists any other person, whether directly or indirectly, to deal with any property—

    for the purpose of—

    • (c) concealing that property; or

    • (d) enabling another person to conceal that property.

    (5) In any prosecution for an offence against subsection (2) or subsection (3),—

    • (a) it is not necessary for the prosecution to prove that the accused knew or believed that the property was the proceeds of a particular specified drug offence or a particular class of specified drug offence:

    • (b) it is no defence that the accused believed any property to be the proceeds of a particular specified drug offence, when in fact the property was the proceeds of another specified drug offence.

    (6) It is a defence to a charge under this section if the act to which the charge relates was done by that person, in good faith, for the purpose of or in connection with—

    • (a) the enforcement or intended enforcement of this section or any other provision of this Act or any other enactment relating to a specified drug offence or any other serious offence; or

    (7) Subject to subsection (8), this section does not apply if—

    • (a) any property is alleged to be the proceeds of a serious offence; and

    • (b) the act that is alleged to constitute that serious offence was committed outside New Zealand; and

    • (c) the act was not, at the time of its commission, an offence under the law of the place where the act was done.

    (8) If a person is charged with an offence against this section and the act that is alleged to constitute the serious offence resulting in proceeds was committed outside New Zealand, it is to be presumed, unless the person charged puts the matter at issue, that the act was an offence under the law of the place where the act was done.

    (9) Nothing in this section limits or restricts the operation of any other provision of this Act or any other enactment.

    Section 12B: inserted, on 12 May 1998, by section 5 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 12B(1) serious offence: amended, on 1 October 2003, by section 34 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 12B(1) specified drug offence paragraph (a): amended, on 22 June 2005, by section 11 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12B(2): substituted, on 1 October 2003, by section 34 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 12B(3): substituted, on 1 October 2003, by section 34 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 12B(6)(b): amended, on 1 December 2009, by section 212 of the Criminal Proceeds (Recovery) Act 2009 (2009 No 8).

    Section 12B(6)(ba): inserted, on 17 October 2009, by section 161(2) of the Anti-Money Laundering and Countering Financing of Terrorism Act 2009 (2009 No 35).

12C Commission of offences outside New Zealand
  • (1) Subject to subsection (2), every person commits an offence against this Act who, outside New Zealand, does or omits to do any act that would, if done or omitted in New Zealand, constitute an offence against—

    (2) No proceedings for an offence against subsection (1) may be brought unless—

    • (a) the person to be charged is a New Zealand citizen; or

    • (b) the person to be charged is present in New Zealand.

    (3) Every person who commits an offence against this section is liable on conviction on indictment to the same penalty to which the person would have been liable had that person committed the offence in New Zealand.

    (4) Subsection (1) does not apply if the doing or omission of the act to which the charge relates was not an offence under the law of the place where the act was done or omitted.

    (5) Despite subsection (4), if a person is charged with an offence against this section, it is to be presumed, unless the person charged puts the matter at issue, that the doing or omission of the act to which the charge relates was an offence under the law of the place where the act was done or omitted.

    (6) Section 28A applies to proceedings for offences against this section.

    Section 12C: inserted, on 12 May 1998, by section 5 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 12C(1)(ca): inserted, on 22 June 2005, by section 12 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

13 Miscellaneous offences
  • (1) Every person commits an offence against this Act who—

    • (a) has in that person’s possession any pipe or other utensil (not being a needle or syringe) for the purpose of the commission of an offence against this Act; or

    • (aa) has in that person’s possession for the purpose of committing an offence under this Act any needle or syringe—

      • (i) that he or she obtained from a person (a supplier) who he or she could not have reasonably believed at the time of the acquisition was a pharmacist, pharmacy employee, approved medical practitioner, or an authorised representative; or

      • (ii) that another person (an acquirer) obtained on his or her behalf from a supplier who the acquirer could not have reasonably believed at the time the needle or syringe was obtained was a pharmacist, pharmacy employee, approved medical practitioner, or an authorised representative; or

      • (iii) other than a needle or syringe that he or she obtained in accordance with any regulations made under section 37 that regulate the sale, exchange, or supply of needles or syringes; or

      • (iv) other than a needle or syringe that the acquirer obtained on his or her behalf in accordance with any regulations made under section 37 that regulate the sale, exchange, or supply of needles or syringes; or

    • (b) except as may be provided by regulations made under this Act, has in his possession the seed or fruit (not in either case being a controlled drug) of any prohibited plant which he is not authorised under this Act to cultivate.

    (2) Subsection (4) of section 9 shall apply in relation to a charge under paragraph (b) of subsection (1) as if, in the said subsection (4), a reference to the seed or fruit of a prohibited plant were substituted for the reference to the prohibited plant.

    (2A) No pharmacist, pharmacy employee, approved medical practitioner, or authorised representative commits an offence by selling or supplying any needle or syringe in accordance with any regulations made under section 37 that regulate the sale, exchange, or supply of needles or syringes.

    (3) Every person who commits an offence against this section is liable to imprisonment for a term not exceeding 1 year or to a fine not exceeding $500 or to both.

    (4) For the purposes of this section, unless the context otherwise requires,—

    approved medical practitioner means a medical practitioner who has been approved by the Director-General of Health under any regulations made under section 37 for the purposes of those regulations

    authorised representative means, in relation to an agency, an association, or a body approved by the Director-General of Health, a person for the time being approved by the Director-General as a representative of that agency, association, or body

    needle means a needle forming part of, or attached to, or designed for attachment to and use with, a syringe

    pharmacy employee means a person employed in a pharmacy within the meaning of the Medicines Act 1981.

    Compare: 1965 No 45 s 7

    Section 13(1)(a): substituted, on 13 January 1988, by section 3 of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Section 13(1)(aa): substituted, on 22 June 2005, by section 13(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 13(2A): inserted, on 22 June 2005, by section 13(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 13(4): added, on 22 June 2005, by section 13(3) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

14 Licences
  • (1) Licences granted under this Act shall be in such form and be subject to such conditions as may be prescribed, or permitted to be designed or imposed, and shall be issued by such persons as may be prescribed, by regulations made under this Act.

    (2) No licence to import into or export from New Zealand opium prepared for smoking shall be granted under this Act.

    (3) Except in the case of a licence issued for the purpose of research or study, no licence granted under this Act shall authorise the consumption, injection, or smoking of any controlled drug.

    (4) Except with the approval of the Minister, no licence shall be granted under this Act to any person who has been convicted of an offence against this Act or any Act repealed by this Act or by the Narcotics Act 1965 or whose licence under any such Act has been revoked by reason of his failure to comply with the conditions thereof or by reason of the breach of the provisions of any such Act or of any regulation made thereunder.

    (5) If at any time the laws of a country or territory prohibit or restrict the importation of a controlled drug into that country or territory, any licence to export that controlled drug from New Zealand may contain conditions calculated to prevent any contravention of those laws in relation to the controlled drug which is the subject of the licence.

    (6) Without prejudice to his liability under any other provision of this Act, every person commits an offence against this Act who contravenes or fails to comply with any condition of a licence granted to him under this Act.

    Compare: 1965 No 45 s 8; SR 1966/82 r 4(8); SR 1973/100 r 3

15 False statements
  • Every person commits an offence against this Act and is liable to imprisonment for a term not exceeding 1 year or to a fine not exceeding $1,000 or to both who, for the purpose of obtaining, whether for himself or any other person, the grant or renewal of any licence under this Act or for any other purpose in relation to this Act,—

    • (a) makes any declaration or statement which to his knowledge is false in any particular; or

    • (b) utters, produces, or makes use of any declaration or statement which to his knowledge is false in any particular; or

    • (c) knowingly utters, produces, or makes use of any document that is not genuine.

    Compare: 1965 No 45 s 9

16 Obstruction of officers
  • Every person commits an offence against this Act who wilfully obstructs, hinders, resists, or deceives any other person in the execution of any powers conferred on that other person by or pursuant to this Act.

    Compare: 1965 No 45 s 10

17 Liability of principal for acts of agent, etc
  • (1) Where an offence is committed against this Act or against any regulation made under this Act by any person acting as the agent or servant of another person, or being otherwise subject to the supervision or instructions of another person for the purposes of any employment in the course of which the offence was committed, that other person shall, without prejudice to the liability of the first mentioned person, be liable under this Act in the same manner and to the same extent as if he had personally committed the offence if it is proved that the act which constituted the offence was committed with his consent or connivance or that it was attributable to any neglect on his part.

    (2) Where any body corporate is convicted of an offence against this Act or against any regulation made under this Act, every director and every person concerned in the management of the company shall be guilty of a like offence if it is proved that the act which constituted the offence was committed with his consent or connivance or that it was attributable to any neglect on his part.

    Compare: 1965 No 45 s 11

18 Search and seizure
  • (1) Where a search warrant is issued under section 198 of the Summary Proceedings Act 1957 in respect of an offence which has been or is suspected to have been committed against this Act or which is believed to be intended to be so committed, any constable executing the warrant or any of his assistants may search any person found in or on the building, aircraft, ship, hovercraft, carriage, vehicle, premises, or place which may be entered and searched under the authority of the warrant.

    (2) Where any constable has reasonable ground for believing that there is in or on any building, aircraft, ship, hovercraft, carriage, vehicle, premises, or place any controlled drug specified or described in Schedule 1 or in Part 1 of Schedule 2 or in Part 1 of Schedule 3 or any precursor substance specified or described in Part 3 of Schedule 4 and that an offence against this Act has been or is suspected of having been committed in respect of that drug or precursor substance, he, and any assistants who accompany him, may enter and search the building, aircraft, ship, hovercraft, carriage, vehicle, premises, or place and any person found therein or thereon as if authorised to do so by a search warrant issued under section 198 of the Summary Proceedings Act 1957 and by subsection (1).

    (3) Where any constable has reasonable ground for believing that any person is in possession of any controlled drug specified or described in Schedule 1 or in Part 1 of Schedule 2 or in Part 1 of Schedule 3 or any precursor substance specified or described in Part 3 of Schedule 4 and that an offence against this Act has been or is suspected of having been committed in respect of that drug or precursor substance, he may search and detain that person for the purpose of search and may take possession of any controlled drug or precursor substance found. Nothing in this subsection shall limit the provisions of subsections (1) and (2) or authorise any constable to enter and search any building, aircraft, ship, hovercraft, carriage, vehicle, premises, or place otherwise than in accordance with the provisions of those subsections.

    (3A) If it is necessary for a constable to stop a vehicle for the purpose of exercising the power conferred by subsection (3) to search a person who is in the vehicle, sections 314B to 314D of the Crimes Act 1961 apply with any necessary modifications as if references in those sections to a statutory search power are references to subsection (3).

    (4) Every constable exercising the power of entry and search conferred by subsection (2) or the power conferred by subsection (3) shall identify himself to every person searched, and also to any person in or on the building, aircraft, ship, hovercraft, carriage, vehicle, premises, or place who questions his right to enter and search the same, and shall also tell those persons that the search is being made pursuant to the authority of that subsection. He shall also, if not in uniform and if so required, produce evidence that he is a constable.

    (5) Any officer of Customs, or any officer of the Ministry of Health, or any Medical Officer of Health, or any constable, with such assistants as he thinks necessary, may seize and destroy any prohibited plant except where it is being cultivated either in accordance with the conditions of a licence granted under this Act or in accordance with regulations made under this Act, and may also seize and destroy the seed of any prohibited plant except where that seed is in the possession of any person who is either authorised under this Act to cultivate the plant or who is permitted by regulations made under this Act to have the seed in his possession.

    (6) Where any constable exercises the power of entry and search conferred by subsection (2) or the power conferred by subsection (3), he shall, within 3 days after the day on which he exercises the power, furnish to the Commissioner of Police a written report on the exercise of the power and the circumstances in which it came to be exercised.

    Compare: 1965 No 45 s 12

    Section 18(2): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 18(2): amended, on 22 June 2005, by section 14(1)(a) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 18(2): amended, on 22 June 2005, by section 14(1)(b) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 18(3): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 18(3): amended, on 22 June 2005, by section 14(2)(a) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 18(3): amended, on 22 June 2005, by section 14(2)(b) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 18(3): amended, on 22 June 2005, by section 14(2)(c) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 18(3A): inserted, on 1 January 1998, by section 25 of the Crimes Amendment Act (No 2) 1997 (1997 No 93).

    Section 18(3A): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 18(4): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 18(5): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 18(5): amended, on 1 July 1993, pursuant to section 38(3) of the Health Amendment Act 1993 (1993 No 24).

    Section 18(5): amended, on 1 July 1993, by section 32 of the Health Reforms (Transitional Provisions) Act 1993 (1993 No 23).

    Section 18(6): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

18A Internal search of person under arrest
  • (1) Notwithstanding anything in section 37 of the Policing Act 2008 or any other enactment or rule of law to the contrary, no constable shall conduct an internal search of any part of the body of any person nor, except in accordance with subsection (2), shall he cause any other person to conduct such a search:

    provided that, with the consent of the person concerned, a constable may search that person’s mouth.

    (2) Where any person (in this section referred to as the suspect) is arrested for any offence against section 6 or section 7 or section 11, a constable who is of or above the level of position of inspector or constable who is of or above the level of position of sergeant but below the level of position of inspector who has reasonable ground for believing that the suspect has secreted within his body any property that may be evidence of the offence with which the suspect is charged, or any property the possession of which by the suspect constitutes any other offence against any of the said provisions, may require the suspect to permit a medical practitioner, nominated for the purpose by the constable, to conduct an internal examination of any part of the suspect’s body by means of an X-ray machine or other similar device, or by means of a manual or visual examination (whether or not facilitated by any instrument or device) through any body orifice.

    (3) Notwithstanding anything in subsection (2) or the terms of any requirement made under that section, no medical practitioner shall conduct any such internal examination if he considers that to do so may be prejudicial to the suspect’s health, or if he is satisfied that the suspect is not prepared to permit an internal examination to be conducted.

    (4) Notwithstanding anything in the Summary Proceedings Act 1957 or this Act, where the suspect fails to permit an internal examination to be conducted under this section and subsequently applies for bail, the court may (without limiting its discretion to refuse bail) decline to consider the application until the expiry of 2 days after the day on which the requirement to do so was made or until the suspect sooner permits such an examination to be conducted, if the court is satisfied that the requirement was properly made on reasonable grounds; and, in any such case, the court may order that the suspect shall continue to be detained in Police custody until the expiry of that period or until the suspect sooner complies, as the case may be.

    (5) Nothing in this section shall limit or affect the provisions of sections 13A to 13M of the Misuse of Drugs Amendment Act 1978.

    Section 18A: inserted, on 12 December 1979, by section 2 of the Misuse of Drugs Amendment Act (No 2) 1979 (1979 No 132).

    Section 18A(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 18A(1): amended, on 1 October 2008, by section 130(1) of the Policing Act 2008 (2008 No 72).

    Section 18A(1) proviso: amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 18A(2): amended, on 1 October 2008, pursuant to section 116(b) of the Policing Act 2008 (2008 No 72).

    Section 18A(2): amended, on 1 October 2008, pursuant to section 116(c) of the Policing Act 2008 (2008 No 72).

    Section 18A(2): amended, on 13 January 1983, by section 4 of the Misuse of Drugs Amendment Act 1982 (1982 No 151).

    Section 18A(5): added, on 1 October 1985, by section 3 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

19 Power to demand production of records and to inspect stocks of controlled drugs
  • (1) Any constable or any other person authorised by the Minister shall for the purposes of the enforcement of the provisions of this Act have power to enter the premises of any person who carries on the business of a producer, manufacturer, seller, or distributor of any controlled drug, or who otherwise undertakes the supply or administration of any controlled drug, and to demand the production of and to inspect any books or documents relating to dealings in any controlled drug, and to inspect, weigh, measure, and record the stocks of controlled drugs.

    (2) If in the opinion of any Medical Officer of Health there is reasonable ground for suspecting that any person is in possession of any controlled drug for the purpose of sale, or for the purpose of manufacturing any preparation for sale, or for use in or in connection with his profession, trade, or calling, or any occupation whether paid or unpaid, in breach of this Act or of any regulations made under this Act, the Medical Officer of Health may require that person to produce for his inspection or to produce to any person specially authorised by the Medical Officer of Health in that behalf, any books or documents dealing with the reception, possession, purchase, sale, or delivery of the controlled drug.

    (3) Any person acting under, or pursuant to an authority under, subsection (1) or subsection (2) may make copies of or extracts from any such books or documents, and the copies or extracts, certified as such by that person, shall be deemed to be true and correct copies or extracts, unless the contrary is proved.

    (4) Every person commits an offence against this Act who refuses or neglects to comply with any demand or requisition made pursuant to this section.

    (5) [Repealed]

    Compare: 1965 No 45 s 13

    Section 19(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 19(5): repealed, on 1 April 1987, by section 25(1) of the Official Information Amendment Act 1987 (1987 No 8).

20 Statements regarding drug dependent persons
  • (1) If a Medical Officer of Health has reason to believe that any person is or is likely to become dependent on any controlled drug, he may, for the purpose of preventing or restricting the supply of controlled drugs to that person, or of assisting in the cure or mitigation or avoidance of the dependence of that person, publish statements relating to that person to all or any of the members of all or any of the classes of persons set out in subsection (3).

    (2) Every statement made under subsection (1) shall be privileged unless the publication is proved to be made with malice.

    (3) The classes of persons referred to in subsection (1) are as follows:

    • (aa) [Repealed]

    • (b) a hospital care operator within the meaning of section 58(4) of the Health and Disability Services (Safety) Act 2001:

    • (e) medical practitioners:

    • (f) dentists:

    • (fa)  midwives:

    • (fb) designated prescribers:

    • (g) Police employees:

    • (h) persons who deal in controlled drugs in the course of business.

    (4) Nothing in subsection (1) or subsection (2) shall limit or affect any right or duty which a Medical Officer of Health may otherwise possess to publish a statement to any person.

    (5) Every person commits an offence against this Act who, except in the course of duty as a member of a class set out in subsection (3) or as an officer or servant of the Crown, publishes any information obtained, whether by him or any other person, from a statement made pursuant to subsection (1), or any comment on any such statement.

    Compare: 1965 No 45 s 20

    Section 20(3)(a): substituted, on 1 January 2001, by section 111(1) of the New Zealand Public Health and Disability Act 2000 (2000 No 91).

    Section 20(3)(aa): repealed, on 1 July 1993, by section 32 of the Health Reforms (Transitional Provisions) Act 1993 (1993 No 23).

    Section 20(3)(b): substituted, on 1 October 2002, by section 58(1) of the Health and Disability Services (Safety) Act 2001 (2001 No 93).

    Section 20(3)(c): substituted, on 1 June 2005, by section 206 of the Corrections Act 2004 (2004 No 50).

    Section 20(3)(fa): inserted, on 28 August 1990, by section 15 of the Nurses Amendment Act 1990 (1990 No 107).

    Section 20(3)(fa): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 20(3)(fb): inserted, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 20(3)(g): amended, on 1 October 2008, by section 130(1) of the Policing Act 2008 (2008 No 72).

21 Power of court to restrict publication of name of controlled drug
  • (1) Where, in the course of proceedings in any court or before a coroner, reference is made to any controlled drug, the court or coroner may in its or his discretion order that the name of that drug shall not be published in relation to those proceedings at any time before the expiration of a period of 5 years from the date of the final disposal of those proceedings:

    provided that no order made under this subsection shall apply to the publication of that name to scientists or to members of the legal, medical, dental, veterinary, nursing, or pharmaceutical professions or to persons studying to become scientists or members of those professions or in any publication of a scientific or technical character solely or mainly intended for circulation among scientists or members of those professions or persons so studying or in any publication published by or on behalf of the Crown.

    (2) Where the publication of the name of a controlled drug is prohibited under this section in relation to any proceedings every person commits an offence against this Act who, within the said period of 5 years, publishes the name of that drug or any name or particulars likely to lead to the identification of that drug as the controlled drug to which reference was made in those proceedings.

    (3) Nothing in this section shall be construed to limit the provisions of any other enactment relating to the prohibition or regulation of the publication of reports or particulars relating to any judicial proceedings.

    Compare: 1965 No 45 s 20A; 1970 No 27 s 5

22 Powers of Minister to prohibit importation, etc, of controlled drugs
  • (1) The Minister may from time to time, by notice in the Gazette, prohibit the import, manufacture, production, procuring, possession, supply, administration, or other use of any specified controlled drug, either absolutely or subject to such conditions as he thinks fit, for any specified period not exceeding 1 year:

    provided that this power shall not be exercised more than once in respect of any controlled drug so specified.

    (1A) The Minister may from time to time, by notice in the Gazette, prohibit the importation, supply, possession for the purpose of sale or supply, or offering for sale of any class of pipe, other utensil, or identifiable component of a pipe or other utensil, not being a needle or syringe, that may be used for administering any controlled drug or in the preparation of any controlled drug to be administered, either absolutely or subject to such conditions as the Minister thinks fit.

    (2) Every person commits an offence against this Act who,—

    • (a) being a person permitted by or under this Act to import, manufacture, produce, procure, possess, supply, administer, or otherwise use, as the case may require, a controlled drug specified in a notice under subsection (1); or

    • (b) were it not for a notice issued under subsection (1), would be permitted by or under this Act to import, manufacture, produce, procure, possess, supply, administer, or otherwise use, as the case may require, a controlled drug specified in that notice,—

    contravenes or fails to comply with that notice.

    (3) Every person commits an offence against this Act who—

    • (a) supplies, possesses for the purpose of sale or supply, or offers for sale a pipe, other utensil, or identifiable component of a pipe or other utensil whose sale, possession for the purpose of sale or supply, or offering for sale (as the case may be) is absolutely prohibited by a notice issued under subsection (1A); or

    • (b) supplies, possesses for the purpose of sale or supply, or offers for sale a pipe, other utensil, or identifiable component of a pipe or other utensil otherwise than in accordance with any condition under which that pipe, other utensil, or identifiable component of a pipe or other utensil may, under a notice issued under subsection (1A), be supplied, possessed for the purpose of sale or supply, or offered for sale (as the case may be); or

    • (c) imports a pipe, other utensil, or identifiable component of a pipe or other utensil otherwise than in accordance with any condition under which that pipe, other utensil, or identifiable component of a pipe or other utensil may, under a notice issued under subsection (1A), be imported.

    (4) Subject to subsection (5), every person who commits an offence against subsection (3) is liable,—

    • (a) in the case of an individual, to imprisonment for a term not exceeding 3 months or to a fine not exceeding $1,000, or to both; or

    • (b) in the case of a body corporate, to a fine not exceeding $5,000.

    (5) Where—

    • (a) a body corporate is convicted of an offence against subsection (3); and

    • (b) under section 17(2), a person (being a director or person concerned in the management of that body corporate) is also guilty of that offence,—

    that person is liable to imprisonment for a term not exceeding 3 months or to a fine not exceeding $5,000, or to both.

    (6) Every notice issued under subsection (1A) is a regulation for the purposes of the Regulations (Disallowance) Act 1989, but is not a regulation for the purposes of the Acts and Regulations Publication Act 1989.

    Compare: 1960 No 97 s 28

    Section 22 heading: amended, on 21 August 1997, by section 2 of the Misuse of Drugs Amendment Act 1997 (1997 No 57).

    Section 22(1A): inserted, on 13 January 1988, by section 4(1) of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Section 22(1A): amended, on 9 August 2011, by section 6(1)(a) of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Section 22(1A): amended, on 9 August 2011, by section 6(1)(b) of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Section 22(2): substituted, on 21 August 1997, by section 2(1) of the Misuse of Drugs Amendment Act 1997 (1997 No 57).

    Section 22(3): substituted, on 9 August 2011, by section 6(2) of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Section 22(4): added, on 21 August 1997, by section 2(1) of the Misuse of Drugs Amendment Act 1997 (1997 No 57).

    Section 22(5): added, on 21 August 1997, by section 2(1) of the Misuse of Drugs Amendment Act 1997 (1997 No 57).

    Section 22(6): added, on 21 August 1997, by section 2(1) of the Misuse of Drugs Amendment Act 1997 (1997 No 57).

23 Powers of Minister to prohibit prescribing, etc
  • (1) Subject to subsection (2), the Minister may at any time, by notice in the Gazette,—

    • (a) prohibit any specified medical practitioner, dentist, midwife, designated prescriber, or veterinarian from prescribing controlled drugs:

    • (aa) prohibit any specified midwife from prescribing pethidine (as described in Schedule 2):

    • (b) prohibit any specified person from exercising all or any of the rights conferred by section 8, whether those rights are so conferred on persons generally or on a particular class of person to which that person belongs.

    (2) The Minister shall not exercise any power conferred on him by subsection (1)—

    • (a) in the case of a medical practitioner, except on the recommendation of the Medical Council of New Zealand; or

    • (b) in the case of a dentist, except on the recommendation of the Dental Council of New Zealand; or

    • (c) in the case of a veterinarian, except on the recommendation of the Veterinary Council of New Zealand; or

    • (ca) in the case of a midwife, except on the recommendation of the Nursing Council of New Zealand; or

    • (d) in the case of a pharmacist, except on the recommendation of the Pharmacy Council; or

    • (e) in the case of any designated prescriber to whom paragraph (d) does not apply, except on the recommendation of the Council or Board, specified in regulations made under this Act, that has jurisdiction in respect of the class of registered health professional to which the designated prescriber belongs.

    (3) The Minister may at any time, by notice in the Gazette, revoke any notice given under subsection (1).

    (4) Notwithstanding anything in any other Act, each Council and each Board referred to in subsection (2) shall, for the purpose of considering and determining whether or not to make a recommendation to the Minister under that subsection, have jurisdiction to inquire into any prescribing of or dealing in controlled drugs by a member of the profession with which it is concerned, and any matter incidental thereto, when such prescribing or dealing has been brought or otherwise comes to its attention.

    (5) For the purposes of subsection (4), each such Council or Board has and may exercise any powers with respect to summoning witnesses, administering oaths, hearing evidence and other matters of procedure, and with respect to the payment and receiving of costs and expenses, conferred on it or any disciplinary committee or disciplinary tribunal, in relation to disciplinary proceedings, by the enactment under which the Council or Board is constituted.

    (5A) Despite subsection (5), it is not necessary, unless the Council or Board so requires, for any other body to conduct an investigation or inquiry or to be represented at the inquiry conducted by the Council or Board.

    (6) Without prejudice to the liability of any person under any other provision of this Act, every medical practitioner, dentist, midwife, designated prescriber, or veterinarian who prescribes any controlled drug in contravention of a notice under subsection (1) commits an offence against this Act and is liable—

    • (a) to imprisonment for a term not exceeding 6 months or to a fine not exceeding $1,000 or to both where a Class A controlled drug or a Class B controlled drug was the controlled drug or one of the controlled drugs in relation to which the offence was committed:

    • (b) to imprisonment for a term not exceeding 3 months or to a fine not exceeding $200 or to both, in any other case.

    (7) Without prejudice to the liability of any midwife under any other provision of this Act, every midwife who prescribes pethidine (as so described) in contravention of a notice under subsection (1) commits an offence against this Act and is liable to imprisonment for a term not exceeding 6 months or to a fine not exceeding $1,000, or to both.

    Compare: SR 1966/82 rr 13(2), 21, 35

    Section 23(1)(a): amended, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 23(1)(a): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 23(1)(a): amended, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 23(1)(aa): inserted, on 28 August 1990, by section 16(1) of the Nurses Amendment Act 1990 (1990 No 107).

    Section 23(1)(aa): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 23(2)(c): amended, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 23(2)(ca): inserted, on 28 August 1990, by section 16(2) of the Nurses Amendment Act 1990 (1990 No 107).

    Section 23(2)(ca): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 23(2)(d): amended, on 22 June 2005, by section 15 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 23(2)(e): added, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 23(4): amended, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 23(5): substituted, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 23(5A): inserted, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 23(6): amended, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 23(6): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 23(6): amended, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 23(7): added, on 28 August 1990, by section 16(3) of the Nurses Amendment Act 1990 (1990 No 107).

    Section 23(7): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

24 Treatment of people dependent on controlled drugs
  • (1) Every medical practitioner commits an offence who prescribes, administers, or supplies a controlled drug for or to a person who the practitioner has reason to believe is dependent on that or any other controlled drug,—

    • (a) in the course or for the purpose of the treatment of the person for dependency; and

    • (b) otherwise than in accordance with subsection (2).

    (1A) Every midwife or designated prescriber commits an offence against this Act who prescribes, administers, or supplies a controlled drug for or to a person who the midwife or prescriber has reason to believe is dependent on that or any other controlled drug, in the course of, or for the purpose of, the treatment of the person for dependency.

    (2) In the course or for the purpose of the treatment for dependency of a person who the practitioner has reason to believe is dependent on that or any other controlled drug, a medical practitioner may prescribe, administer, or provide a controlled drug for or to the person if the medical practitioner—

    • (a) is for the time being specified under subsection (7)(a); or

    • (b) is—

      • (i) working in an institution, clinic, or place for the time being specified under subsection (7)(b); and

      • (ii) for the time being authorised in writing to prescribe controlled drugs by a medical practitioner working in that institution, clinic, or place who is for the time being specified under subsection (7)(a); and

    • (c) is—

      • (i) acting in the medical practitioner’s capacity as a medical officer employed by a hospital care operator within the meaning of section 58(4) of the Health and Disability Services (Safety) Act 2001 for the time being specified under subsection (7)(b); and

      • (ii) for the time being authorised in writing by the person in charge of that institution, acting under the general or specific directions of a Medical Officer of Health, to prescribe controlled drugs; or

    • (d) is acting—

      • (i) with the permission in writing, given in relation to that particular person, of a medical practitioner for the time being authorised by paragraph (a) or paragraph (b) or paragraph (c) to do so; and

      • (ii) during the period, and in accordance with the terms and conditions (if any), specified or imposed in the permission, or in any written modification of the permission, given by that medical practitioner.

    (3) Except with the concurrence of the Medical Officer of Health, no permission under subsection (2)(d) may specify a period longer than 3 months.

    (4) A permission under subsection (2)(d) may from time to time be renewed by the person who gave it, or any other medical practitioner authorised by that paragraph to give such a permission.

    (5) Except with the concurrence of the Medical Officer of Health, no renewal under subsection (4) of a permission under subsection (2)(d) may be for a period longer than 3 months.

    (6) An authority or permission given or renewed under subsection (2) or subsection (4)—

    • (a) may at any time be withdrawn by the person who gave or renewed it, by written notice to the person to whom it was given; and

    • (b) is deemed to have been withdrawn when, as the case may be,—

      • (i) the notice under subsection (7)(a) specifying the medical practitioner by whom the authority or permission was given is revoked; or

      • (ii) the notice under subsection (7)(b) specifying the institution, clinic, or place, in respect of which the authority or permission concerned was given or renewed is revoked; or

      • (iii) the medical practitioner by whom the authority or permission was given dies, or ceases to work in the premises, clinic, or place to which the authority relates.

    (7) The Minister may from time to time, by notice in the Gazette,—

    • (a) specify any medical practitioner (by name) as a medical practitioner who may, subject to any general or specific conditions imposed by the Minister on the recommendation of the Director-General of Health, prescribe, administer, or supply controlled drugs for the purposes of this section:

    • (b) specify (by name or description) as a place at which controlled drugs may be prescribed, administered, or supplied for the purposes of this section—

      • (i) any hospital care institution within the meaning of section 58(4) of the Health and Disability Services (Safety) Act 2001; or

      • (ii) any clinic, or other place in which a medical practitioner for the time being specified under paragraph (a) works.

    (8) The Minister may from time to time, by notice in the Gazette, revoke or amend a notice under subsection (7).

    (9) This section does not apply to—

    • (b) the emergency treatment of a patient in a hospital care institution within the meaning of section 58(4) of the Health and Disability Services (Safety) Act 2001, for a period not exceeding 3 days:

    • (c) the treatment of any restricted person within the meaning of section 25.

    Section 24: substituted, on 1 October 2002, by section 58(1) of the Health and Disability Services (Safety) Act 2001 (2001 No 93).

    Section 24(1A): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 24(1A): amended, on 22 October 2003, by section 4(1) of the Misuse of Drugs Amendment Act 2003 (2003 No 86).

    Section 24(7)(a): amended, on 22 October 2003, by section 4(2) of the Misuse of Drugs Amendment Act 2003 (2003 No 86).

25 Restrictions on supply to particular persons
  • (1) In this section restricted person means a person who is the subject of a notice given under subsection (3) and for the time being in force.

    (2) Every person commits an offence against this Act who,—

    • (a) in contravention of a notice which has been served on him pursuant to subsection (3) or subsection (4), or which has otherwise come to his attention, prescribes for or supplies to a restricted person, knowing him to be a restricted person, any controlled drug; or

    • (b) knowing himself to be a restricted person, procures or attempts to procure a prescription or a controlled drug from a person who is for the time being prohibited, by a notice under subsection (3) or subsection (4), from issuing the prescription or supplying the controlled drug to him.

    (3) Where a Medical Officer of Health is satisfied that any person has been obtaining a controlled drug over a prolonged period and is likely to seek further supplies of a controlled drug, or prescriptions for the supply of a controlled drug, he may from time to time, by notice in such form as he thinks fit, given generally or to any person authorised by or under this Act to supply controlled drugs, prohibit every medical practitioner and dentist from issuing prescriptions for the supply of, and every person from supplying, any controlled drugs to the first-mentioned person, subject to such exceptions, relating to particular medical practitioners or dentists or sources of supply, or particular controlled drugs, or the frequency or quantity of prescriptions or supply, as may be specified in the notice.

    (4) The Medical Officer of Health may at any time by a like notice revoke, or vary, or modify any prohibition, condition, or exception contained in a notice given by him under this section.

    (5) A copy of any notice under subsection (3) or subsection (4) shall be served, either personally or by registered post, on the restricted person, but failure to comply with this requirement shall not invalidate the notice.

    (6) Any person who is aggrieved by the issue of a notice under this section, or by the refusal of the Medical Officer of Health to revoke, vary, or modify, any prohibition, condition, or exception contained in any such notice, may appeal in writing to the Minister whose decision shall be final.

    Compare: SR 1966/82 rr 13(2), 26

26 Arrest by Customs officers
  • If any officer of Customs has reasonable cause to believe or suspect that any person, in contravention of this Act, has imported into or exported from New Zealand any controlled drug, or has been concerned in such import or export, he may arrest that person without a warrant.

    Compare: 1965 No 45 s 14

27 General penalty
  • Every person who commits an offence against this Act for which no penalty is provided elsewhere than in this section is liable to imprisonment for a term not exceeding 3 months or to a fine not exceeding $500 or to both.

    Compare: 1965 No 45 s 15

28 Legal proceedings
  • (1) Except where this Act otherwise provides, every offence against this Act or against any regulations made under this Act shall be punishable on summary conviction.

    (2) Notwithstanding anything in section 14 of the Summary Proceedings Act 1957, any information in respect of any offence against this Act or against any regulations made under this Act may be laid at any time within 4 years from the time when the matter of the information arose.

    (2A) Notwithstanding anything in section 14 of the Summary Proceedings Act 1957 or subsection (2), any information in respect of any offence against section 6 or section 9 or section 10 may be laid at any time.

    (3) Amendment(s) incorporated in the Act(s).

    Compare: 1965 No 45 s 16

    Section 28(2A): inserted, on 7 January 1981, by section 2 of the Misuse of Drugs Amendment Act 1980 (1980 No 64).

28A Consent of Attorney-General required in proceedings under section 12C
  • (1) No information may be laid for an offence against section 12C except with the consent of the Attorney-General.

    (2) A person who is alleged to have committed an offence against section 12C may be arrested, or a warrant for the arrest of the person may be issued and executed, and any such person may be remanded in custody or on bail, even if the Attorney-General’s consent to the laying of the information has not been obtained, but no further or other proceedings may be taken until that consent has been obtained.

    (3) The Attorney-General may, before deciding whether or not to give his or her consent under subsection (1), make such inquiries as he or she thinks fit.

    Section 28A: inserted, on 12 May 1998, by section 6 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

29 Mistake as to nature of controlled drug or precursor substance
  • Where, in any proceedings for an offence against any of the provisions of section 6 or section 7 or section 12A or section 12AB or section 12AC, it is necessary, if the defendant is to be convicted of the offence charged, for the prosecution to prove that some substance, preparation, mixture, or article involved in the alleged offence was the controlled drug or precursor substance which the prosecution alleges it to have been, and it is proved that the substance, preparation, mixture, or article was that controlled drug or precursor substance, the defendant shall not be acquitted of the offence charged by reason only of the fact that he did not know or may not have known that the substance, preparation, mixture, or article in question was the particular controlled drug or precursor substance alleged.

    Section 29 heading: amended, on 12 May 1998, by section 7 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 29: amended, on 22 June 2005, by section 16 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 29: amended, on 12 May 1998, by section 7(a) of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 29: amended, on 12 May 1998, by section 7(b) of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

29A Issue of usable quantity
  • (1) On the summary trial of any person charged with an offence against this Act in which it is alleged that the defendant had in his possession any controlled drug in contravention of this Act, it shall not be necessary for the prosecution to prove that the amount of the controlled drug in the defendant’s possession was of a usable quantity, unless the defendant puts the matter in issue.

    (2) Where, in the course of a summary trial, the defendant puts in issue the question of whether or not the amount of any controlled drug alleged to have been in his possession was of a usable quantity, the District Court Judge shall, if requested to do so by the prosecutor, adjourn the hearing for such period as he considers sufficient to enable the prosecutor to arrange for the attendance in court of a witness or witnesses to adduce evidence that that amount was of a usable quantity; and, if the prosecutor has closed his case before the said question is put in issue, the District Court Judge shall also grant the prosecutor leave to re-open his case for the purpose of adducing evidence that the amount of the drug was of a usable quantity.

    Section 29A: inserted, on 16 October 1978, by section 7 of the Misuse of Drugs Amendment Act 1978 (1978 No 65).

    Section 29A(2): amended, on 1 April 1980, pursuant to section 18(2) of the District Courts Amendment Act 1979 (1979 No 125).

29B Special provisions where offence relating to cannabis preparations alleged
  • For the purposes of any proceedings for an offence against any of the provisions of section 6 or section 7 in relation to any cannabis preparation the following provisions shall apply:

    • (a) it shall be for the prosecution to prove that the preparation to which the charge relates contains any tetrahydrocannabinols:

    • (b) subject to paragraph (a), the preparation shall be deemed to have been produced by subjecting cannabis plant material to some kind of processing unless it is in a form that is clearly recognisable as plant material:

    • (c) plant material means the whole or any part of the leaf, flower, or stalk of any plant (of whatever species):

    • (d) the question of whether or not any preparation is in a form that is clearly recognisable as plant material shall, in the event of dispute between the prosecutor and the defendant, be determined by the jury (or, if there is no jury, by the Judge as a question of fact) by means of a visual inspection unaided by any microscope or magnifying glass (other than spectacles ordinarily worn) or by any other device.

    Section 29B: inserted, on 13 January 1983, by section 6 of the Misuse of Drugs Amendment Act 1982 (1982 No 151).

29C Special provisions where offence relating to controlled drug analogues alleged
  • It shall be a defence to a charge relating to the possession of any controlled drug analogue in contravention of any of the provisions of this Act if the defendant proves that he or she had the substance—

    • (a) for some purpose other than—

      • (i) consuming, smoking, snorting, or injecting by any person, or using in any other manner intended to have a pharmacological effect on the user; and

      • (ii) supplying or administering it to any other person; or

    • (b) for the purpose of supplying it or administering it to any other person in accordance with any procedure approved by the Director-General of Health.

    Section 29C: inserted, on 13 January 1988, by section 5 of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

30 Burden of proof
  • Without prejudice to subsection (8) of section 67 of the Summary Proceedings Act 1957, in any proceedings against any person in respect of any offence against this Act or against any regulations made under this Act in which it is proved that he had in his possession any controlled drug, or did any act in relation to a controlled drug which would have amounted to that offence if such act were not done pursuant to section 8 or to a licence under this Act or as otherwise permitted by regulations under this Act, the burden of proving that he had such controlled drug in his possession, or did such act, pursuant to the said section 8 or to any such licence or as so permitted shall lie on him.

    Compare: 1965 No 45 s 17

31 Evidence of analysis
  • (1) For the purposes of this section, the term analyst means—

    • (a) any person who is designated by the Minister by notice in the Gazette as the analyst in charge of an approved laboratory; or

    • (b) any person who works in an approved laboratory and who is authorised, by the analyst in charge of that laboratory, to act as an analyst for the purposes of this Act, either generally or in any particular case.

    (2) Subject to subsections (3) and (4), in any proceedings for an offence against this Act, a certificate purporting to be signed by an analyst, and certifying that, on a date stated in the certificate, the substance, preparation, mixture, or article to which the certificate relates was received by the signatory personally in any case or (where the substance, preparation, mixture, or article was delivered in a sealed package using a traceable system) by any other person (being a person who works in an approved laboratory and who is authorised, by the analyst in charge of that laboratory, to receive it), from the member of the Police or employee of the Police Department or officer of Customs named in the certificate, and that upon analysis that substance, preparation, mixture, or article was found to be or to contain a particular controlled drug or precursor substance (whether of a specified or an unspecified weight) or a particular prohibited plant, or a particular part of a particular prohibited plant, or a seed or fruit of a particular prohibited plant, specified or described in the certificate, shall until the contrary is proved be sufficient evidence—

    • (a) of the qualifications and authority of the person by whom the analysis was carried out; and

    • (b) of the authority of the person who signed the certificate to sign that certificate; and

    • (c) of the facts stated in the certificate.

    (2A) Where the substance, preparation, mixture, or article was delivered in a sealed package using a traceable system and received by any person (not being the person who signed the certificate but being a person who works in an approved laboratory and who is authorised, by the analyst in charge of that laboratory, to receive it) from any person referred to in subsection (2),—

    • (a) the person who made the analysis may give evidence of receipt by that other person of the substance, preparation, mixture, or article that is the subject of the analysis; and

    • (b) such evidence shall, in the absence of evidence to the contrary, be admissible as sufficient proof of the proper receipt of the substance, preparation, mixture, or article by the person who made the analysis.

    (3) A certificate referred to in subsection (2) shall be admissible in evidence only if—

    • (a) at least 7 clear days before the hearing at which the certificate is tendered, a copy of that certificate is served, by or on behalf of the prosecutor, on the defendant and the defendant is at the same time informed in writing that the prosecutor does not propose to call the person who made the analysis as a witness at the hearing; and

    • (b) the defendant does not, by notice in writing given to the prosecutor at least 3 clear days before the hearing, require the person who made the analysis to be called by the prosecutor as a witness at the hearing.

    (4) Notwithstanding anything in subsection (3), a certificate referred to in subsection (2) shall not be admissible in evidence if the court, either of its own motion or on the application of the defendant made either before or after the commencement of the hearing, in its discretion directs that the result of the analysis shall be disregarded unless that result is proved by the oral evidence of the person who made the analysis.

    (5) In this section—

    member of the Police includes the following persons:

    • (a) a member of the Royal New Zealand Naval Police:

    • (b) a member of the New Zealand Army Military Police:

    • (c) a member of the Senior Air Security Specialist trade, or of the Air Security Specialist trade, of the Royal New Zealand Air Force:

    • (d) an officer of the Air Security specialisation of the Operational Support Branch of the Royal New Zealand Air Force

    served means served in accordance with sections 24 to 29 of the Summary Proceedings Act 1957.

    (6) Any notice given by the Minister in the Gazette for the purposes of subsection (1) shall be deemed to be a regulation for the purposes of the Regulations (Disallowance) Act 1989 and the Interpretation Act 1999.

    Section 31(1): substituted, on 1 July 1992, by section 5(1) of the Misuse of Drugs Amendment Act 1992 (1992 No 49).

    Section 31(2): substituted, on 13 January 1988, by section 6(1) of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Section 31(2): amended, on 7 July 2010, by section 4(1) of the Misuse of Drugs Amendment Act 2010 (2010 No 72).

    Section 31(2): amended, on 12 May 1998, by section 8 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 31(2): amended, on 1 July 1992, by section 5(2) of the Misuse of Drugs Amendment Act 1992 (1992 No 49).

    Section 31(2A): substituted, on 1 July 1992, by section 5(3) of the Misuse of Drugs Amendment Act 1992 (1992 No 49).

    Section 31(2A): amended, on 7 July 2010, by section 4(2) of the Misuse of Drugs Amendment Act 2010 (2010 No 72).

    Section 31(5): added, on 7 January 1981, by section 3(2) of the Misuse of Drugs Amendment Act 1980 (1980 No 64).

    Section 31(5) member of the Police: substituted, on 22 October 2003, by section 5 of the Misuse of Drugs Amendment Act 2003 (2003 No 86).

    Section 31(5) member of the Police paragraph (c): substituted, on 27 March 2008, by section 4 of the Misuse of Drugs Amendment Act 2008 (2008 No 13).

    Section 31(5) member of the Police paragraph (d): substituted, on 27 March 2008, by section 4 of the Misuse of Drugs Amendment Act 2008 (2008 No 13).

    Section 31(6): added, on 1 July 1992, by section 5(4) of the Misuse of Drugs Amendment Act 1992 (1992 No 49).

    Section 31(6): amended, on 1 November 1999, pursuant to section 38(1) of the Interpretation Act 1999 (1999 No 85).

32 Forfeiture
  • (1) Every person convicted of an offence against this Act shall, in addition to any penalty imposed pursuant to this Act, forfeit to Her Majesty, by virtue of such conviction, all articles, if any, in respect of which the offence was committed and in the possession of such person.

    (2) Articles forfeited under the provisions of subsection (1) shall be sold, destroyed, or otherwise disposed of as the Minister directs.

    (3) If, on the conviction of any person for an offence against section 6, the Judge or District Court Judge is satisfied that money found in the possession of that person was received by that person in the course of or consequent upon the commission of that offence, or was in the possession of that person for the purpose of facilitating the commission of an offence against that section, the Judge or District Court Judge may, in addition to any other penalty imposed pursuant to this Act, order that that money be forfeited to the Crown.

    (4) If, on the conviction of any person for an offence against section 6, the court is satisfied that any motor vehicle, aircraft, or ship or boat or other vessel owned by the convicted person (whether solely or as joint tenant or tenant in common with any other person or persons) or in which he has any interest (whether pursuant to a hire purchase agreement, leasing agreement, or otherwise) at the time of his conviction was used by the convicted person in the commission of that offence (whether or not he was the driver or person in charge), the court shall, unless in the circumstances of the case the court considers that it would be unjust to do so, order, in addition to any other penalty imposed under this Act, that the motor vehicle, aircraft, or ship or boat or other vessel be forfeited to Her Majesty.

    (5) If an order for forfeiture is made under subsection (4), the following provisions of the Sentencing Act 2002 apply, so far as they are applicable and with any necessary or specific modifications:

    • (d) section 137, except that paragraphs (c) and (d) of subsection (3) do not apply and, instead, any proceeds of sale remaining after payment in accordance with subsection (3)(a) and (b) must be paid into a Crown Bank Account:

    Compare: 1965 No 45 s 18

    Section 32(3): amended, on 1 April 1980, pursuant to section 18(2) of the District Courts Amendment Act 1979 (1979 No 125).

    Section 32(4): added, on 7 January 1981, by section 4 of the Misuse of Drugs Amendment Act 1980 (1980 No 64).

    Section 32(5): substituted, on 7 July 2004, by section 19 of the Sentencing Amendment Act 2004 (2004 No 68).

    Section 32(5)(d): amended, on 25 January 2005, pursuant to section 65R(3) of the Public Finance Act 1989 (1989 No 44).

33 Notification of conviction of medical practitioners, etc
  • Where any person being a medical practitioner, pharmacist, dentist, midwife, designated prescriber, or veterinarian is convicted of any offence against this Act or against any regulations made under this Act, the court shall cause particulars of the conviction to be sent to the person charged with the duty of keeping the register on which the name of the convicted person appears as a medical practitioner, pharmacist, dentist, midwife, designated prescriber, or veterinarian, as the case may be.

    Compare: 1965 No 45 s 19

    Section 33: amended, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 33: amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 33: amended, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 33: amended, on 28 August 1990, by section 17 of the Nurses Amendment Act 1990 (1990 No 107).

34 Protection of persons acting under authority of Act
  • A person who does any act in pursuance or intended pursuance of any of the functions conferred on him by or under this Act shall not be under any civil or criminal liability in respect thereof, whether on the ground of want of jurisdiction, or mistake of law or fact, or on any other ground, unless he has acted in bad faith or without reasonable care.

    Compare: 1965 No 45 s 21

34A Protection of constables
  • (1) In this section the term undercover officer means a constable whose identity is for the time being concealed for the purpose of a particular investigation of any suspected offence against this Act or of any person suspected of such an offence; and includes any other constable who is for the time being directing or assisting that constable in the course of that investigation.

    (2) No prosecution for an offence against this Act, or against any regulations made under this Act, shall be commenced or continued against any constable in respect of any act committed by him at a time or during a period when he was acting as an undercover officer, except with the leave of the Attorney-General.

    (3) A certificate signed by the Commissioner of Police to the effect that, at any specified time or during any specified period, the constable named in the certificate was acting as an undercover officer shall, for the purposes of subsection (2), be conclusive evidence of that fact.

    Section 34A: inserted, on 16 October 1978, by section 9 of the Misuse of Drugs Amendment Act 1978 (1978 No 65).

    Section 34A heading: amended, on 1 October 2008, pursuant to section 116(a)(iv) of the Policing Act 2008 (2008 No 72).

    Section 34A(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 34A(2): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 34A(3): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

35 Crimes deemed to be included in extradition treaties
  • (1) For the purposes of the Extradition Act 1999 and any Order in Council in force under section 15 or section 104 of that Act,—

    • (a) each crime described in section 6 or section 9, including—

      • (i) attempting or conspiring to commit that crime; or

      • (ii) aiding, abetting, inciting, counselling, or procuring any person to commit that crime; and

    if not already described in the treaty, is deemed to be an offence described in any extradition treaty referred to in subsection (2).

    (2) Subsection (1) applies to any treaty concluded before 1 June 1977 and for the time being in force between New Zealand and any country which is a party to the Single Convention on Narcotic Drugs 1961, as amended by the Protocol amending that Convention, done at Geneva on 25 March 1972, or to the Convention on Psychotropic Substances 1971.

    (3) If under subsection (1) a crime is deemed to be an offence described in an extradition treaty, a person may be surrendered in accordance with the provisions of the Extradition Act 1999 for that crime even if the act or omission occurred before the date on which the crime was deemed to be an offence described in the extradition treaty.

    (4) Subsection (3) does not apply in respect of an act or omission that, had it occurred within the jurisdiction of New Zealand, would not at that time have constituted an offence under New Zealand law.

    (5) For the purposes of this section, country includes any territory for whose international relations the Government of a country is responsible and to which the extradition treaty and the Single Convention on Narcotic Drugs as amended by the Protocol amending that Convention or, as the case may be, the Convention on Psychotropic Substances, extends.

    Section 35: substituted, on 1 September 1999, by section 111 of the Extradition Act 1999 (1999 No 55).

35A Further provision on crimes to be treated as included in extradition treaties
  • (1) For the purposes of the Extradition Act 1999 and any Order in Council in force under section 15 or section 104 of that Act, every offence described in any of sections 6, 9, 12A, 12AB, 12B, and 12C (including attempting or conspiring to commit that offence, aiding, abetting, inciting, counselling, or procuring any person to commit that offence) and every offence described in section 10, if not already described in the treaty, is to be treated as being an offence described in any extradition treaty concluded before the commencement of this section and for the time being in force between New Zealand and any foreign country which is a party to the Vienna Convention.

    (2) When subsection (1) requires any offence to be treated as being an offence described in an extradition treaty, a person whose surrender is sought under the Extradition Act 1999 in respect of an act or omission which amounts to that offence is liable to be surrendered in accordance with the provisions of that Act, whether the act or omission occurred before or after the date on which the offence became, by virtue of subsection (1), an offence described in the extradition treaty.

    (3) This section does not apply in respect of an act or omission that, had it occurred within the jurisdiction of New Zealand, would not at that time have constituted an offence under New Zealand law.

    (4) For the purposes of this section, foreign country includes any territory for whose international relations the Government of a foreign country is responsible and to which the extradition treaty and the Vienna Convention extend.

    Section 35A: inserted, on 16 March 1999, by section 10 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 35A(1): amended, on 22 June 2005, by section 17 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 35A(1): amended, on 1 September 1999, by section 111 of the Extradition Act 1999 (1999 No 55).

    Section 35A(2): amended, on 1 September 1999, by section 111 of the Extradition Act 1999 (1999 No 55).

    Section 35A(3): substituted, on 1 September 1999, by section 111 of the Extradition Act 1999 (1999 No 55).

35B Surrender of offenders
  • [Repealed]

    Section 35B: repealed, on 1 September 1999, by section 111 of the Extradition Act 1999 (1999 No 55).

35C Restrictions on surrender of offenders
  • (1) Without limiting the grounds on which surrender must or may be refused under the Extradition Act 1999, but subject to subsection (2), no court in New Zealand may order the surrender, or the detention for the purposes of surrender, of a person to another country in respect of any act or omission that amounts to an offence described in any of sections 6, 9, 10, 12A, 12AB, 12B, and 12C if the Attorney-General certifies that the case is being or is about to be considered to determine whether or not proceedings should be brought in New Zealand against that person in respect of the act or omission.

    (2) If, in any case to which subsection (1) applies, it is subsequently determined that proceedings should not be brought in New Zealand against the person in respect of the act or omission, the Attorney-General must advise the court accordingly, and the court must proceed with the matter as if the Attorney-General’s certificate had never been given.

    Section 35C: substituted, on 1 September 1999, by section 111 of the Extradition Act 1999 (1999 No 55).

    Section 35C(1): amended, on 22 June 2005, by section 18 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

35D Evidence
  • For any purpose in connection with this Act, a certificate, given by the Secretary of Foreign Affairs and Trade certifying—

    • (a) that any country is or is not, or was or was not at any material time, a party to—

      • (i) the Single Convention on Narcotic Drugs 1961, as amended by the Protocol amending that Convention, done at Geneva on 25 March 1972; or

      • (ii) the Convention on Psychotropic Substances 1971; or

      • (iii) the Vienna Convention; or

    • (b) that the Government of any country is or is not, or was or was not, at any material time, responsible for the international relations of any territory,—

    is sufficient evidence of that fact.

    Section 35D: inserted, on 16 March 1999, by section 10 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

36 Application of Customs and Excise Act 1996
  • (1) Sections 137, 139, 140, 143 to 145, 148 to 149B, 149C(1) and (2), 149D, 151, 152, 161, 165 to 172, 225, and 226 of the Customs and Excise Act 1996 apply in relation to the controlled drugs and precursor substances referred to in subsection (2) as if they were prohibited imports or exports under that Act.

    (2) The controlled drugs and precursor substances are—

    • (a) any controlled drug, other than a controlled drug specified or described in Part 6 of Schedule 3; and

    • (b) any precursor substance specified or described in Schedule 4.

    Section 36: substituted, on 22 June 2005, by section 19 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

37 Regulations
  • (1) The Governor-General may from time to time, by Order in Council, make regulations for all or any of the following purposes:

    • (a) providing for the issue of licences for the import, export, possession, production, manufacture, procuring, supply, administration, or use of controlled drugs and the cultivation of prohibited plants:

    • (b) prescribing the form, duration, terms, and conditions of any licence under this Act and enabling additional conditions to be imposed:

    • (c) prescribing the fees payable for licences under this Act and providing for the cancellation and suspension of such licences:

    • (d) permitting the import, export, possession, production, manufacture, procuring, supply, administration, or use of controlled drugs, and the cultivation of prohibited plants, otherwise than pursuant to a licence under this Act but subject to such conditions or restrictions as may be prescribed by or imposed under the regulations:

    • (e) prohibiting, limiting, restricting, and imposing conditions on, either generally or in relation to particular cases or classes of case or particular classes of person, the prescribing, production, manufacture, procuring, supply, use, or possession of controlled drugs pursuant to any provision of section 8:

    • (f) requiring persons who are engaged in the import, export, production, manufacture, procuring, supply, or administration of any controlled drug, or who utilise any controlled drug in the course of or in connection with their profession, trade, or calling, or any occupation whether paid or unpaid, or who otherwise undertake the supply or administration of any controlled drug, to keep records in such form and manner and to furnish information with respect to such matters as may be prescribed:

    • (fa) regulating the issue of standing orders that authorise the supply and administration of controlled drugs, imposing conditions, limitations, requirements, or restrictions in relation to the contents of standing orders of that kind and their use, and providing for any other matters that are necessary or desirable for the administration of standing orders of that kind:

    • (g) regulating the issue by medical practitioners, dentists, midwives, designated prescribers, and veterinarians of prescriptions for the supply of any controlled drug, and requiring persons issuing or dispensing prescriptions in respect of any such drug to furnish such information relating to those prescriptions as may be prescribed:

    • (ga) prescribing the circumstances in which, and the conditions under which, any person or class of persons may possess needles or syringes notwithstanding that those needles or syringes may be intended to be used for the purpose of the commission of offences against this Act:

    • (gb) regulating the sale, exchange, or supply of needles or syringes—

      • (i) by medical practitioners or pharmacists generally, or by those approved for the purpose by the Director-General of Health; or

      • (ii) by authorised representatives of any agency, association, or body approved for the purpose by the Director-General of Health,—

      notwithstanding that those needles or syringes may be intended by the persons to whom they are sold or supplied, or with whom they are exchanged, to be used for the commission of offences against this Act:

    • (h) requiring any medical practitioner who attends a person whom he considers, or has reasonable grounds to suspect, is dependent on controlled drugs of any description to furnish such particulars with respect to that person as may be prescribed:

    • (i) prohibiting, regulating, or restricting the supply of controlled drugs to any person so dependent and the issue of prescriptions for such supply:

    • (j) regulating the dispensing and compounding of controlled drugs:

    • (k) regulating the packing, labelling, storage, carriage, and destruction of controlled drugs:

    • (l) declaring plants to be prohibited plants:

    • (m) controlling or restricting the cultivation and destruction of prohibited plants and the sale, distribution, possession, and destruction of the seeds or fruit of prohibited plants:

    • (n) providing for the weighing, counting, measuring, sealing, seizing, and taking of samples of controlled drugs:

    • (o) prohibiting, regulating, or restricting advertisements for controlled drugs, and statements made in any such advertisement:

    • (p) providing for the waiver of fees in whole or in part in particular cases or classes of cases and for the total or partial refund of fees:

    • (q) prescribing offences in respect of the contravention of or non-compliance with any regulations made under this Act, and the amounts of fines that may be imposed in respect of any such offences, which fines shall be an amount not exceeding $500 and, where the offence is a continuing one, a further amount not exceeding $20 for every day or part of a day during which the offence has continued:

    • (r) exempting, or providing for the exemption of, any persons or classes of persons, or excepting any controlled drugs, from any provision of any regulation made under this Act which imposes conditions or obligations:

    • (s) generally for prohibiting, controlling, or restricting the import, export, possession, production, manufacture, procuring, supply, administration, and use of controlled drugs:

    • (t) providing for such matters as are contemplated by or necessary for giving full effect to the provisions of this Act and for its due administration.

    (2) Any regulations made under subsection (1) may—

    • (a) be expressed to apply to controlled drugs generally, or to particular controlled drugs or classes of controlled drugs specified or described in the regulations, and may make different provision for different controlled drugs or classes of controlled drugs so specified or described:

    • (b) provide for depriving persons of any rights, privileges, or exemptions, conferred on any class of person to which those persons belong, by any such regulations.

    Compare: 1965 No 45 s 23; 1960 No 97 s 53(2)(h), (o); Misuse of Drugs Act 1971 s 10(2)(g), (h), (i) (UK)

    Section 37(1)(fa): inserted, on 22 October 2003, by section 6 of the Misuse of Drugs Amendment Act 2003 (2003 No 86).

    Section 37(1)(g): amended, on 22 December 2005, by section 105 of the Veterinarians Act 2005 (2005 No 126).

    Section 37(1)(g): amended, on 18 September 2004, by section 175(1) of the Health Practitioners Competence Assurance Act 2003 (2003 No 48).

    Section 37(1)(g): amended, on 15 October 1999, by section 16 of the Medicines Amendment Act 1999 (1999 No 117).

    Section 37(1)(g): amended, on 28 August 1990, by section 18 of the Nurses Amendment Act 1990 (1990 No 107).

    Section 37(1)(ga): inserted, on 13 January 1988, by section 7 of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Section 37(1)(gb): inserted, on 13 January 1988, by section 7 of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

38 Effect on Poisons Act 1960
  • [Repealed]

    Section 38: repealed, on 2 July 2001, by section 149 of the Hazardous Substances and New Organisms Act 1996 (1996 No 30).

39 Repeals
  • (1) The Narcotics Act 1965 and the Narcotics Amendment Act 1970 are hereby repealed.

    (2) Any reference in any enactment or in any document to a narcotic within the meaning of the Narcotics Act 1965 shall hereafter, unless the context otherwise requires, be read as a reference to a controlled drug within the meaning of this Act.

40 Revocations
  • The following Orders in Council are hereby revoked, namely:

    • (a) the Narcotics Order 1966:

    • (b) the Narcotics Order 1967:

    • (c) the Narcotics Order (No 2) 1967:

    • (d) the Narcotics Order 1968.

41 Application to Niue
  • Amendment(s) incorporated in the Act(s).


Schedule 1
Class A controlled drugs

s 2(1)

1 The following substances, namely:
  • Acetorphine (03-acetyl-7,8-dihydro-7 α-[1 (R)-hydroxy-1-methylbutyl]-06-methyl-6,14-endoethenomorphine)

    Bufotenine (3-(2-dimethylaminoethyl)-5-hydroxyindole)

    Cantharidin (hexahydro-3a,7a-dimethyl-4,7-epoxyisobenzofuran-1,3-dione)

    Cocaine (methyl ester of benzoylecgonine), except when contained in a Class C controlled drug

    Desomorphine (dihydrodeoxymorphine)

    DET (N,N-diethyltryptamine)

    DMA (2-amino-1-(2,5-dimethoxyphenyl)propane)

    DMHP (3-(1,2-dimethylheptyl)-1-hydroxy-7,8,9,10-tetrahydro-6,6,9-trimethyl-6H-dibenzo [b,d] pyran)

    DMT (N,N-dimethyltryptamine)

    DOB (2-amino-1-(4-bromo-2,5-dimethoxyphenyl)propane) (also known as bromo-DMA)

    Etorphine (7,8-dihydro-7 α-[1 (R)-hydroxy-1-methylbutyl]-06-methyl-6,14-endoethenomorphine)

    Heroin (diacetylmorphine)

    Ketobemidone (4-meta-hydroxyphenyl-1-methyl-4-propionylpiperidine)

    Lysergic acid (essential precursor for manufacture of LSD)

    Lysergide (N,N-diethyllysergamide or lysergic acid diethylamide)

    MDA (2-amino-1-(3,4-methylenedioxyphenyl) propane)

    Mescaline (3,4,5-trimethoxyphenethylamine)

    Methamphetamine (2-methylamino-1-phenylpropane)

    5-methoxydimethyltryptamine (5-methoxy-N,N-dimethyltryptamine)

    2-methoxy-4,5-methylenedioxyamphetamine (2-amino-1-(2-methoxy-4,5-methylenedioxyphenyl) propane) (also known as MMDA or MMDA-2)

    3-methoxy-4,5-methylenedioxyamphetamine (2-amino-1-(3-methoxy-4,5-methylenedioxyphenyl) propane) (also known as MMDA)

    MPTP (1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine)

    Parahexyl (3-hexyl-1-hydroxy-7,8,9,10-tetrahydro-6,6,9-trimethyl-6H-dibenzo [b,d] pyran)

    PCE (N-ethyl-1-phenylcyclohexylamine)

    PCPY (1-(1-phenylcyclohexyl)pyrrolidine)

    PEPTP (1-(2-phenylethyl)-4-phenyl-1,2,5,6-tetrahydropyridine)

    Phencyclidine (1-(1-phenylcyclohexyl) piperidine)

    PHP (1-(1-phenylcyclohexyl)pyrrolidine)

    Piperidyl benzilates (N-methylpiperidyl benzilates and N-ethylpiperidyl benzilates but excluding the methobromide salts)

    PMA (2-amino-1-(4-methoxyphenyl)propane)

    Psilocine (3-(2-dimethylaminoethyl)-4-hydroxyindole)

    Psilotsin (3-(2-dimethylaminoethyl)-4-hydroxyindole)

    Psilocybine (3-(2-dimethylaminoethyl) indol-4-yl dihydrogen phosphate)

    STP,DOM (2-amino-1-(2,5-dimethoxy-4-methyl) phenylpropane)

    TCP (1-[1-(2-thienyl)cyclohexyl]piperidine)

    TMA (2-amino-1-(3,4,5-trimethoxyphenyl)propane).

    Schedule 1 clause 1 4-bromo-2,5-dimethoxyamphetamine: repealed, on 2 September 1996, by section 6(1)(a) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 Cocaine: inserted, on 13 January 1988, by section 8 of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Schedule 1 clause 1 2,5-dimethoxyamphetamine: repealed, on 2 September 1996, by section 6(1)(b) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 DMA: inserted, on 2 September 1996, by section 6(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 DOB: inserted, on 2 September 1996, by section 6(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 Lysergic acid: inserted, on 2 September 1996, by section 6(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 Methamphetamine: inserted, on 30 May 2003, by clause 4 of the Misuse of Drugs (Changes to Controlled Drugs) Order 2003 (SR 2003/47).

    Schedule 1 clause 1 4-methoxyamphetamine: repealed, on 2 September 1996, by section 6(1)(c) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 2-methoxy-4,5-methylenedioxyamphetamine: inserted, on 2 September 1996, by section 6(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 3-methoxy-4,5-methylenedioxyamphetamine: substituted, on 2 September 1996, by section 6(2) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 MPTP: inserted, on 13 January 1988, by section 8 of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Schedule 1 clause 1 PCE: inserted, on 21 May 1981, by clause 2 of the Misuse of Drugs Order 1981 (SR 1981/114).

    Schedule 1 clause 1 PCPY: inserted, on 21 May 1981, by clause 2 of the Misuse of Drugs Order 1981 (SR 1981/114).

    Schedule 1 clause 1 PEPTP: inserted, on 13 January 1988, by section 8 of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Schedule 1 clause 1 PHP: inserted, on 21 May 1981, by clause 2 of the Misuse of Drugs Order 1981 (SR 1981/114).

    Schedule 1 clause 1 PMA: inserted, on 2 September 1996, by section 6(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 TCP: inserted, on 21 May 1981, by clause 2 of the Misuse of Drugs Order 1981 (SR 1981/114).

    Schedule 1 clause 1 Tetrahydrocannabinols: repealed, on 2 September 1996, by section 6(1)(d) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 Thalidomide: repealed, on 9 August 2011, by section 7 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Schedule 1 clause 1 TMA: inserted, on 2 September 1996, by section 6(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 1 clause 1 3,4,5-trimethoxyamphetamine: repealed, on 2 September 1996, by section 6(1)(e) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

2
  • The isomers of the substances mentioned in this schedule whenever the existence of such isomers is possible within the specific chemical designation.

3
  • The esters and ethers of the substances mentioned in this schedule and the esters and ethers of the isomers mentioned in clause 2 whenever the existence of such esters or ethers is possible.

4
  • The salts of the substances mentioned in this schedule and the salts of the isomers, esters, and ethers mentioned in clause 2 or clause 3.

5

Schedule 2
Class B controlled drugs

s 2(1)

Part 1

1 The following substances, namely:
  • Amphetamine (2-amino-1-phenylpropane)

    Cannabis preparations: that is, any preparation containing any tetrahydrocannabinols, including cannabis resin (commonly known as hashish) and cannabis oil (commonly know as hash oil), produced by subjecting cannabis plant material to any kind of processing

    MDMA (2-methylamino-1-(3,4-methylenedioxyphenyl) propane)

    Methcathinone

    Morphine

    Opium

    Tetrahydrocannabinols, except when contained in a Class C controlled drug.

    Schedule 2 Part 1 clause 1 Amphetamine: inserted, on 9 September 2005, by clause 4(1) of the Misuse of Drugs (Changes to Controlled Drugs) Order 2005 (SR 2005/175).

    Schedule 2 Part 1 clause 1 Cannabis: substituted, on 13 January 1983, by section 7 of the Misuse of Drugs Amendment Act 1982 (1982 No 151).

    Schedule 2 Part 1 clause 1 Cocaine: repealed, on 13 January 1988, by section 9(1) of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Schedule 2 Part 1 clause 1 MDMA: inserted, on 9 September 2005, by clause 4(1) of the Misuse of Drugs (Changes to Controlled Drugs) Order 2005 (SR 2005/175).

    Schedule 2 Part 1 clause 1 Methcathinone: inserted, on 30 May 2003, by clause 5(1) of the Misuse of Drugs (Changes to Controlled Drugs) Order 2003 (SR 2003/47).

    Schedule 2 Part 1 clause 1 Tetrahydrocannabinols: added, on 2 September 1996, by section 7(1) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

2
  • The isomers of the substances mentioned in clause 1 whenever the existence of such isomers is possible within the specific chemical designation.

    Schedule 2 Part 1 clause 2: amended, on 31 May 2002, by clause 3(2)(a) of the Misuse of Drugs (Classification of Fantasy) Order 2001 (SR 2001/383).

3
  • The esters and ethers of the substances mentioned in clause 1 and the esters and ethers of the isomers mentioned in clause 2 whenever the existence of such esters or ethers is possible.

    Schedule 2 Part 1 clause 3: amended, on 31 May 2002, by clause 3(2)(b) of the Misuse of Drugs (Classification of Fantasy) Order 2001 (SR 2001/383).

4
  • The salts of the substances mentioned in clause 1 and the salts of the isomers, esters, and ethers mentioned in clause 2 or clause 3.

    Schedule 2 Part 1 clause 4: amended, on 31 May 2002, by clause 3(2)(c) of the Misuse of Drugs (Classification of Fantasy) Order 2001 (SR 2001/383).

5
6
  • The substance gamma-hydroxybutyrate (GHB) (commonly known as fantasy) and—

    • (a) the esters, ethers, and amides of GHB; and

    • (b) all substances from which GHB can be derived, including (without limitation)—

      • (i) 1,4-butanediol:

      • (ii) gamma-aminobutyric acid:

      • (iii) gamma-butyrolactone:

      • (iv) gamma-hydroxybutyraldehyde; and

    • (c) the salts of GHB (including sodium oxybate) and the salts of any substance referred to in paragraph (a) or paragraph (b); and

    • (d) any substance, preparation, or mixture containing any proportion of GHB or any substance referred to in any of paragraphs (a) to (c).

    Schedule 2 Part 1 clause 6: added, on 31 May 2002, by clause 3(1) of the Misuse of Drugs (Classification of Fantasy) Order 2001 (SR 2001/383).

Part 2

1 The following substances, namely:
  • Benzphetamine (2-benzylmethylamino-1-phenylpropane)

    Cathinone (2-amino-1-phenylpropan-1-one)

    DOET (2-amino-1-(2,5-dimethoxy-4-ethylphenyl) propane)

    Ephedrine

    N-ethyl MDA (2-ethylamino-1-(3,4-methylenedioxyphenyl) propane)

    N-ethylamphetamine (2-ethylamino-1-phenylpropane)

    Fencamfamine (N-ethyl-3-phenylbicyclo[2.2.1]heptan-2-amine)

    Fenethylline (3,7-dihydro-1,3-dimethyl-7-[2-[(1-methyl-2-phenylethyl)-amino]ethyl]-1H-purine-2,6-dione)

    Fenproporex (2-(2-cyanoethylamino)-1-phenylpropane)

    N-hydroxy MDA (2-hydroxyamino-1-(3,4-methylenedioxyphenyl) propane)

    Mefenorex (2-(3-chloropropylamino)-1-phenylpropane)

    Methaqualone (2-methyl-3-(2-methylphenyl)-4(3H)-quinazolinone)

    4-methylaminorex (cis-2-amino-4-methyl-5-phenyl-2-oxazoline)

    Methylphenidate (α-phenyl-2-piperidineacetic acid methyl ester)

    4-methylthioamphetamine

    Norpseudoephedrine (threo-2-amino-1-hydroxy-1-phenylpropane), including cathine

    Propylhexedrine (1-cyclohexyl-2-methylaminopropane)

    Pseudoephedrine

    Pyrovalerone (1-(4-methylphenyl)-2-(1-pyrrolidinyl)-1-pentanone).

    Schedule 2 Part 2 clause 1: substituted, on 13 January 1988, by section 9(2) of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Schedule 2 Part 2 clause 1 Amphetamine: repealed, on 9 September 2005, by clause 4(2) of the Misuse of Drugs (Changes to Controlled Drugs) Order 2005 (SR 2005/175).

    Schedule 2 Part 2 clause 1 Ephedrine: inserted, on 8 September 2011, by section 8 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Schedule 2 Part 2 clause 1 N-ethyl MDA: inserted, on 2 September 1996, by section 7(3) of the Misuse of Drugs Amendment Act 1996 (1966 No 133).

    Schedule 2 Part 2 clause 1 N-hydroxy MDA: inserted, on 2 September 1996, by section 7(3) of the Misuse of Drugs Amendment Act 1996 (1966 No 133).

    Schedule 2 Part 2 clause 1 MDMA: repealed, on 9 September 2005, by clause 4(2) of the Misuse of Drugs (Changes to Controlled Drugs) Order 2005 (SR 2005/175).

    Schedule 2 Part 2 clause 1 Methamphetamine: repealed, on 30 May 2003, by clause 5(2) of the Misuse of Drugs (Changes to Controlled Drugs) Order 2003 (SR 2003/47).

    Schedule 2 Part 2 clause 1 4-methylaminorex: inserted, on 2 September 1996, by section 7(3) of the Misuse of Drugs Amendment Act 1996 (1966 No 133).

    Schedule 2 Part 2 clause 1 4-methylthioamphetamine: inserted, on 30 May 2003, by clause 5(3) of the Misuse of Drugs (Changes to Controlled Drugs) Order 2003 (SR 2003/47).

    Schedule 2 Part 2 clause 1 Norpseudoephedrine: substituted, on 2 September 1996, by section 7(2) of the Misuse of Drugs Amendment Act 1996 (1966 No 133).

    Schedule 2 Part 2 clause 1 Pseudoephedrine: inserted, on 8 September 2011, by section 8 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

2
  • The isomers of the substances mentioned in this Part whenever the existence of such isomers is possible within the specific chemical designation.

3
  • The esters and ethers of the substances mentioned in this Part and the esters and ethers of the isomers mentioned in clause 2 whenever the existence of such esters or ethers is possible.

4
  • The salts of the substances mentioned in this Part and the salts of the isomers, esters, and ethers mentioned in clause 2 or clause 3.

5

Part 3

1 The following substances, namely:
  • Acetyl-α-methylfentanyl (N-[1-(α-methylphenethyl]-4-piperidyl] acetanilide)

    Acetylmethadol (3-acetoxy-6-dimethylamino-4,4-diphenylheptane)

    Alfentanil (N-[1-[2-(4-ethyl-4,5-dihydro-5-oxo-1H-(tetrazol-1-yl)ethyl]-4-(methoxymethyl)-4-piperidinyl]-N-phenylpropanamide)

    Allylprodine (3-allyl-1-methyl-4-phenyl-4-propionoxypiperidine)

    Alphacetylmethadol (α-3-acetoxy-6-dimethylamino-4,4-diphenylheptane)

    Alphameprodine (α-3-ethyl-1-methyl-4-phenyl-4-propionoxypiperidine)

    Alphamethadol (α-6-dimethylamino-4,4-diphenyl-3-heptanol)

    Alphaprodine (α-1,3-dimethyl-4-phenyl-4-propionoxypiperidine)

    Anileridine (1-para-aminophenethyl-4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Benzethidine (1-(2-benzyloxyethyl)-4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Benzylmorphine (3-benzylmorphine)

    Betacetylmethadol (β-3-acetoxy-6-dimethylamino-4,4-diphenylheptane)

    Betameprodine (β-3-ethyl-1-methyl-4-phenyl-4-propionoxypiperidine)

    Betamethadol (β-6-dimethylamino-4,4-diphenyl-3-heptanol)

    Betaprodine (β-1,3-dimethyl-4-phenyl-4-propionoxypiperidine)

    Bezitramide (1-(3-cyano-3,3-diphenylpropyl)-4-(2-oxo-3-propionyl-1-benzimidazolinyl)piperidine)

    Clonitazene (2-para-chlorbenzyl-1-diethylaminoethyl-5-nitrobenzimidazole)

    Codoxime (dihydrocodeinone-6-carboxymethyloxime)

    Concentrate of poppy straw—that is, the material arising when parts of any plant of the speciesPapaver somniferum have entered a process for the concentration of the alkaloids

    Dextromoramide ((+)-4-[2-methyl-4-oxo-3,3-diphenyl-4-(1-pyrrolidinyl) butyl] morpholine)

    Diampromide (N-[2-(methylphenethylamino) propyl] propionanilide)

    Diethylthiambutene (3-diethylamino-1,1-di-(2′-thienyl)-1-butene).

    Difenoxin (1-(3-cyano-3, 3 diphenylpropyl)-4-phenylisonipecotic acid)

    Dihydromorphine

    Dimenoxadol (2-dimethylaminoethyl 1-ethoxy-1, 1-diphenylacetate)

    Dimepheptanol (6-dimethylamino-4,4-diphenyl-3-heptanol)

    Dimethylthiambutene (3-dimethylamino-1,1-di-(2′-thienyl)-1-butene)

    Dioxaphetyl butyrate (ethyl 4-morpholino-2, 2-diphenylbutyrate)

    Diphenoxylate (1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Dipipanone (4,4-diphenyl-6-piperidine-3-heptanone)

    Drotebanol (3,4-dimethoxy-17-methylmorphinan-6β, 14-diol)

    Ecgonine, its esters and derivatives which are convertible to ecgonine and cocaine, except when contained in a Class C controlled drug

    Ethylmethylthiambutene (3-ethylmethylamino-1,1-di-(2′-thienyl)-1-butene)

    Etonitazene (1-diethylaminoethyl-2-para-ethoxybenzyl-5-nitrobenzimidazole)

    Etoxeridine (1-[2-(2-hydroxyethoxy)ethyl]-4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Fentanyl (1-phenethyl-4-(N-propionylanilino)piperidine)

    p-fluorofentanyl (4′-fluoro-N-1-(phenethyl-4-piperidyl) propionanilide)

    Furethidine (1-(2-tetrahydrofurfuryloxyethyl)-4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Hydrocodone (dihydrocodeinone)

    Hydromorphinol (14-hydroxydihydromorphine)

    Hydromorphone (dihydromorphinone)

    β-hydroxyfentanyl (N-[1-(β-hydroxyphenethyl)-4-piperidyl] propionanilide)

    β-hydroxy-3-methylfentanyl (N-[1-(β-hydroxyphenethyl)-3-methyl-4-piperidyl]propionanilide)

    Hydroxypethidine (4-meta-hydroxyphenyl-1-methylpiperidine-4-carboxylic acid ethyl ester)

    Isomethadone (6-dimethylamino-5-methyl-4,4-diphenyl-3-hexanone)

    Levomethorphan ((−)-3-methoxy-N-methylmorphinan) but not including dextromethorphan ((+)-3-methoxy-N-methylmorphinan) and dextrorphan ((+)-3-hydroxy-N-methylmorphinan)

    Levomoramide ((−)-4-[2-methyl-4-oxo-3,3-diphenyl-4-(1-pyrrolidinyl) butyl] morpholine)

    Levophenacylmorphan ((−)-3-hydroxy-N-phenacylmorphinan)

    Levorphanol ((−)-3-hydroxy-N-methylmorphinan)

    Mecloqualone (3-(2-chlorophenyl)-2-methyl-4-(3H)-quinazolinone)

    Metazocine (2′-hydroxy-2,5,9-trimethyl-6,7-benzomorphan)

    Methadone (6-dimethylamino-4,4-diphenyl-3-heptanone)

    Methadone-intermediate (4-cyano-2-dimethylamino-4,4-diphenylbutane)

    1-methyl-4-phenyl-4-piperidinol

    Methyldesorphine (6-methyl-Δ6-deoxymorphine)

    Methyldihydromorphine (6-methyldihydromorphine)

    α-methylfentanyl (N-[1-(α-methylphenethyl)-4-piperidyl]propionanilide)

    3-methylfentanyl (N-[3-methyl-1-phenethyl-4-piperidyl] propionanilide)

    α-methylthiofentanyl (N-[1-[1-methyl-2-(2-thienyl)ethyl]-4-piperidyl]propionanilide)

    3-methylthiofentanyl (N-[3-methyl-1-[2-(2-thienyl)ethyl]-4-piperidyl]propionanilide)

    Metopon (5-methyldihydromorphinone)

    Moramide-intermediate (2-methyl-3-morpholino-1,1-diphenylpropane carboxylic acid)

    Morpheridine (1-(2-morpholinoethyl)-4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Morphine methobromide and other pentavalent nitrogen morphine derivatives

    Morphine-n-oxide

    MPPP (1-methyl-4-phenyl-4-piperidinol propionate (ester))

    Myrophine (myristylbenzylmorphine)

    Nabilone (trans-3-(1-1-dimethylheptyl)-6,6a,7,8,10,10a-hexahydro-1-hydroxy-6, 6-dimethyl-9H-dibenzo[b,d] pyran-9-one)

    Nicomorphine (3,6-dinicotinylmorphine)

    Noracymethadol (α-3-acetoxy-6-methylamino-4,4-diphenylheptane)

    Norlevorphanol ((−)-3-hydroxymorphinan)

    Normethadone (6-dimethylamino-4,4-diphenyl-3-hexanone)

    Normorphine (demethylmorphine)

    Norpipanone (4,4-diphenyl-6-piperidino-3-hexanone)

    Oxycodone (14-hydroxydihydrocodeinone)

    Oxymorphone (14-hydroxydihydromorphinone)

    PEPAP (1-phenethyl-4-phenyl-4-piperidinol acetate (ester))

    Pethidine (1-methyl-4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Pethidine-intermediate-A (4-cyano-1-methyl-4-phenylpiperidine)

    Pethidine-intermediate-B (4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Pethidine-intermediate-C (1-methyl-4-phenylpiperidine-4-carboxylic acid)

    Phenadoxone (6-morpholino-4,4diphenyl-3-heptanone)

    Phenampromide (N-(1-methyl-2-piperidinoethyl) propionanilide)

    Phenazocine (2′-hydroxy-5,9-dimethyl-2-phenethyl-6,7-benzomorphan)

    Phendimetrazine (3,4-dimethyl-2-phenylmorpholine)

    1-phenethyl-4-phenyl-4-piperidinol.

    Phenmetrazine (3-methyl-2-phenylmorpholine)

    Phenomorphan (3-hydroxy-N-phenethylmorphinan)

    Phenoperidine (1-(3-hydroxy-3-phenylpropyl)-4-phenylpiperidine-4-carboxylic acid ethyl ester)

    Piminodine (4-phenyl-1-(3-phenylaminopropyl)piperidine-4-carboxylic acid ethyl ester)

    Piritramide (1-(3-cyano-3,3-diphenylpropyl)-4-(1-piperidino) piperidine-4-carboxylic acid amide)

    Proheptazine (1,3-dimethyl-4-phenyl-4-propionoxyazacycloheptane)

    Properidine (1-methyl-4-phenylpiperidine-4-carboxylic acid isopropyl ester)

    Racemethorphan ((±)-3-methoxy-N-methylmorphinan)

    Racemoramide ((±) -4- [2-methyl-4-oxo-3, 3-diphenyl-4-(1-pyrrolidinyl) butyl] morpholine)

    Racemorphan ((±)-3-hydroxy-N-methylmorphinan)

    Remifentanil (1-(2-methoxycarbornyl-ethyl)-4-(phenylpropionyl-amino)-piperidine-4-carboxylic acid methyl ester)

    Sufentanil (N-[4-(methoxymethyl)-1-[2-(2-thienyl)ethyl]-4-piperidyl] propionanilide)

    Thebacon (acetyldihydrocodeinone)

    Thebaine

    Thiofentanyl (N-[1-[2-(2-thienyl)ethyl]-4-piperidyl]propionanilide)

    Tilidine ((±)-ethyl trans-2-(dimethylamino)-1-phenyl-3-cyclohexene-1-carboxylate)

    Trimeperidine (1,2,5-trimethyl-4-phenyl-4-propionoxypiperidine).

    Schedule 2 Part 3 clause 1 Acetyl-α-methylfentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 Alfentanil: inserted, on 6 November 1986, by section 4 of the Misuse of Drugs Amendment Act 1986 (1986 No 102).

    Schedule 2 Part 3 clause 1 p-fluorofentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 β-hydroxyfentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 β-hydroxy-3-methylfentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 Mecloqualone: inserted, on 21 May 1981, by clause 3(2) of the Misuse of Drugs Order 1981 (SR 1981/114).

    Schedule 2 Part 3 clause 1 1-methyl-4-phenyl-4-piperidinol: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 α-methylfentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 3-methylfentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 α-methylthiofentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 3-methylthiofentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 MPPP: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 Nabilone: inserted, on 13 January 1988, by section 9(3) of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

    Schedule 2 Part 3 clause 1 PEPAP: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 1-phenethyl-4-phenyl-4-piperidinol: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 Remifentanil: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 Sufentanil: inserted, on 21 May 1981, by clause 3(2) of the Misuse of Drugs Order 1981 (SR 1981/114).

    Schedule 2 Part 3 clause 1 Thiofentanyl: inserted, on 2 September 1996, by section 7(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 2 Part 3 clause 1 Tilidine: inserted, on 21 May 1981, by clause 3(2) of the Misuse of Drugs Order 1981 (SR 1981/114).

2
  • The isomers of the substances mentioned in this Part whenever the existence of such isomers is possible within the specific chemical designation.

3
  • The esters and ethers of the substances mentioned in this Part and the esters and ethers of the isomers mentioned in clause 2 whenever the existence of such esters or ethers is possible.

4
  • The salts of the substances mentioned in this Part and the salts of the isomers, esters, and ethers mentioned in clause 2 or clause 3.

5

Schedule 3
Class C controlled drugs

s 2(1)

Part 1

1
  • Cannabis fruit

    Cannabis plant (whether fresh, dried, or otherwise)—that is, any part of any plant of the genus Cannabis except a part from which all the resin has been extracted

    Cannabis seed

    Catha edulis plant

    Coca leaf—that is, the leaf of any plant of any species of the genus Erythroxylon, except a leaf from which all ecgonine, cocaine, and any other ecgonine alkaloids have been removed.

    Schedule 3 Part 1 clause 1 Cannabis plant: amended, on 13 January 1983, by section 8 of the Misuse of Drugs Amendment Act 1982 (1982 No 151).

    Schedule 3 Part 1 clause 1 Catha edulis plant: inserted, on 21 May 1981, by clause 4 of the Misuse of Drugs Order 1981 (SR 1981/114).

2
  • The following substances:

    BZP (1-benzylpiperazine or A2 benzylpiperazine or N-benzylpiperazine (1-benzyl-1,4-diazacyclohexane))

    TFMPP (1-(3-trifluoromethylphenyl)piperazine or N-(3-trifluoromethylphenyl)piperazine)

    pFPP (1-(4-fluorophenyl)piperazine)

    MeOPP (1-(4-methoxyphenyl)piperazine)

    mCPP (1-(meta-chlorophenyl)piperazine) or 1-(3-chlorophenyl)piperazine)

    MBZP (1-methyl-4-benzylpiperazine).

    Schedule 3 Part 1 clause 2: added, on 1 April 2008, by section 4 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

3
  • The isomers of the substances mentioned in clause 2 whenever the existence of such isomers is possible within the specific chemical designation.

    Schedule 3 Part 1 clause 3: added, on 1 April 2008, by section 4 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

4
  • The esters and ethers of the substances mentioned in clause 2 and the esters and the ethers of the isomers mentioned in clause 3 whenever the existence of such esters or ethers is possible.

    Schedule 3 Part 1 clause 4: added, on 1 April 2008, by section 4 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

5
  • The salts of the substances mentioned in clause 2 and the salts of the isomers, esters, and ethers mentioned in clause 3 or 4.

    Schedule 3 Part 1 clause 5: added, on 1 April 2008, by section 4 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

6
  • Substances containing any proportion of a substance mentioned in clause 2, 3, 4, or 5.

    Schedule 3 Part 1 clause 6: added, on 1 April 2008, by section 4 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

Part 2

Codeine (3-methylmorphine); its isomers, esters, and ethers, if any; its salts, and the salts of its isomers, esters, or ethers, if any; and any substance, preparation or mixture containing any proportion of the said substance or of any such isomer, ester, ether, or salt, other than a preparation or mixture named or described in Part 6

Dihydrocodeine; its isomers, esters, and ethers, if any; its salts, and the salts of its isomers, esters, or ethers, if any; and any substance, preparation, or mixture containing any proportion of the said substance or of any such isomer, ester, ether, or salt, other than a preparation or mixture named or described in Part 6

Propoxyphene (α-4 (N, N-dimethylamino)-1, 2-diphenyl-3-methyl-2-propionoxybutane); its isomers, esters, and ethers, if any; its salts and the salts of its isomers, esters, or ethers, if any; except in preparations of propoxyphene described in clause 5A of Part 5.

  • Schedule 3 Part 2 Dihydrocodeine: inserted, on 2 September 1996, by section 8(1) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

  • Schedule 3 Part 2 Dihydrocodeine amended, on 15 November 2000, by section 10 of the Misuse of Drugs Amendment Act 2000 (2000 No 47).

  • Schedule 3 Part 2 Propoxyphene: substituted, on 20 December 1984, by clause 2(1) of the Misuse of Drugs Order (No 2) 1984 (SR 1984/315).

Part 3

1 The following substances, namely:
  • Acetyldihydrocodeine

    Ethylmorphine (3-ethylmorphine)

    Nicocodine (6-nicotinylcodeine)

    Nicodicodine (6-nicotinyldihydrocodeine or nicotinic acid ester of dihydrocodeine

    Norcodeine (N-demethylcodeine)

    Pholcodine (morpholinylethylmorphine)

    Propiram (N-(1-methyl-2-piperidinoethyl)-N-2-pyridylpropionamide).

    Schedule 3 Part 3 clause 1 Dihydrocodeine: repealed, on 2 September 1996, by section 8(2) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

2
  • The isomers of the substances mentioned in this Part whenever the existence of such isomers is possible within the specific chemical designation.

3
  • The esters and ethers of the substances mentioned in this Part and the esters and the ethers of the isomers mentioned in clause 2 whenever the existence of such esters or ethers is possible.

4
  • The salts of the substances mentioned in this Part and the salts of the isomers, esters, and ethers mentioned in clause 2 or clause 3.

5
6 
  • [Repealed]

    Schedule 3 Part 3 clause 6: repealed, on 8 September 2011, by section 9(1) of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

Part 4

1 The following substances, namely:
  • Allobarbital (5,5-diallylbarbituric acid)

    Amobarbital (5-ethyl-5-(3-methylbutyl) barbituric acid)

    Buprenorphine (17-cyclopropylmethyl-7,8-dihydro-7-(1-hydroxy-1,2, 2-trimethylpropyl) -6-0-methyl-6, 14-ethano-17-normorphine)

    Butalbital (5-allyl-5-isobutylbarbituric acid)

    Butobarbitone (5-butyl-5-ethylbarbituric acid)

    Cyclobarbital (5-(1-cyclohexen-1-yl)-5-ethylbarbituric acid)

    Glutethimide (2-ethyl-2-phenylglutarimide)

    Ketamine (2-(2-chlorophenyl)-2-(methylamino)-cyclohexanone)

    Nealbarbitone (5-allyl-5-neopentylbarbituric acid)

    Pentobarbital (5-ethyl-5-(1-methylbutyl) barbituric acid)

    Secbutabarbital (5-sec-butyl-5-ethylbarbituric acid)

    Secobarbital (5-allyl-5-(1-methylbutyl) barbituric acid)

    Vinylbital (5-(1-methylbutyl)-5-vinylbarbituric acid).

    Schedule 3 Part 4 clause 1 Allobarbital: inserted, on 2 September 1996, by section 8(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 3 Part 4 clause 1 Buprenorphine: substituted, on 26 April 1984, by clause 2 of the Misuse of Drugs Order 1984 (SR 1984/101).

    Schedule 3 Part 4 clause 1 Butalbital: inserted, on 2 September 1996, by section 8(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 3 Part 4 clause 1 Ketamine: inserted, on 1 December 2010, by clause 3 of the Misuse of Drugs (Presumption of Supply—Ketamine) Order 2009 (SR 2009/256)

    Schedule 3 Part 4 clause 1 Secbutabarbital: inserted, on 2 September 1996, by section 8(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

    Schedule 3 Part 4 clause 1 Vinylbital: added, on 2 September 1996, by section 8(3) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).

2
  • The isomers of the substances mentioned in this Part whenever the existence of such isomers is possible within the specific chemical designation.

3
  • The esters and ethers of the substances mentioned in this Part and the esters and the ethers of the isomers mentioned in clause 2 whenever the existence of such esters or ethers is possible.

4
  • The salts of the substances mentioned in this Part and the salts of the isomers, esters, and ethers mentioned in clause 2 or clause 3.

5
  • Substances containing any proportion of a substance mentioned in clause 1, clause 2, clause 3, or clause 4, except a mixture of a derivative of barbituric acid named or described in clause 1 compounded with 1 or more other pharmacologically active ingredients not named or described in clause 1.

    Schedule 3 Part 4 clause 5: amended, on 25 May 1978, by clause 2(1) of the Misuse of Drugs Order 1978 (SR 1978/143).

Part 5

1 The following substances, namely:
  • Alprazolam

    Amfepramone (2-(diethylamino) propiophenone)

    Aminorex

    Barbital (5,5-diethylbarbituric acid)

    Bromazepam

    Brotizolam

    Camazepam

    Chlordiazepoxide

    Clobazam

    Clonazepam

    Clorazepate

    Clotiazepam

    Cloxazolam

    Delorazepam

    Diazepam

    Estazolam

    Ethchlorvynol (ethyl-2-chlorovinylethynyl-carbinol)

    Ethinamate (1-ethynylcyclohexanol carbamate)

    Ethyl loflazepate

    Fludiazepam

    Flunitrazepam

    Flurazepam

    Halazepam

    Haloxazolam

    Ketazolam

    Loprazolam

    Lorazepam

    Lormetazepam

    Mazindol (5-(4-chlorophenyl)-2, 5-dihydro-3H-imidazo [2, 1-a]-isoindol-5-ol)

    Medazepam

    Meprobamate (2-methyl-2-propyl-1,3-propanediol dicarbamate)

    Methylphenobarbital (5-ethyl-1-methyl-5-phenylbarbituric acid)

    Methylprylon (3,3-diethyl-5-methylpiperidine-2,4-dione)

    Midazolam

    Nimetazepam

    Nitrazepam

    Nordazepam

    Oxazepam

    Oxazolam

    Pemoline

    Phenobarbital (5-ethyl-5-phenylbarbituric acid)

    Phentermine (2-amino-2-methyl-1-phenylpropane)

    Pinazepam

    Pipradrol (1,1-diphenyl-1-(2-piperidyl)methanol)

    Prazepam

    SPA ((−)-1-dimethylamino-1,2-diphenylethane)

    Temazepam

    Tetrazepam

    Triazolam.

    Schedule 3 Part 5 clause 1 Alprazolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Aminorex: inserted, on 30 May 2003, by clause 6 of the Misuse of Drugs (Changes to Controlled Drugs) Order 2003 (SR 2003/47).

    Schedule 3 Part 5 clause 1 Bromazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Brotizolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Camazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Chlordiazepoxide: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Clobazam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Clonazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Clorazepate: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Clotiazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Cloxazolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Delorazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Diazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Ephedrine: repealed, on 8 September 2011, by section 9(2) of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Schedule 3 Part 5 clause 1 Estazolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Ethyl loflazepate: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Fludiazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Flunitrazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Flurazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Halazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Haloxazolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Ketazolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Loprazolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Lorazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Lormetazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Mazindol: substituted, on 20 December 1984, by clause 2(2) of the Misuse of Drugs Order (No 2) 1984 (SR 1984/315).

    Schedule 3 Part 5 clause 1 Medazepam: inserted, on 1  January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Midazolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Nimetazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Nitrazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Nordazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Oxazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Oxazolam: inserted, on 1  January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Pemoline: inserted, on 30 May 2003, by clause 6 of the Misuse of Drugs (Changes to Controlled Drugs) Order 2003 (SR 2003/47).

    Schedule 3 Part 5 clause 1 Phentermine: inserted, on 16 December 1982, by clause 2(2) of the Misuse of Drugs Order 1982 (SR 1982/259).

    Schedule 3 Part 5 clause 1 Pinazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Prazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Pseudoephedrine: repealed, on 8 September 2011, by section 9(2) of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Schedule 3 Part 5 clause 1 Temazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Tetrazepam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

    Schedule 3 Part 5 clause 1 Triazolam: inserted, on 1 January 1999, by clause 2 of the Misuse of Drugs Order 1998 (SR 1998/351).

2
  • The isomers of the substances mentioned in this Part whenever the existence of such isomers is possible within the specific chemical designation.

3
  • The esters and ethers of the substances mentioned in this Part and the esters and ethers of the isomers mentioned in clause 2 whenever the existence of such esters or ethers is possible.

4
  • The salts of the substances mentioned in this Part and the salts of the isomers, esters, and ethers mentioned in clause 2 or clause 3.

5
  • Mixtures of a derivative of barbituric acid named or described in Part 4 compounded with 1 or more other pharmacologically active ingredients not named or described in Part 4.

    Schedule 3 Part 5 clause 5: substituted, on 25 May 1978, by clause 2(2) of the Misuse of Drugs Order 1978 (SR 1978/143).

5A
  • Preparations of propoxyphene, its isomers, esters, and ethers, if any, its salts, and the salts of its isomers, esters, or ethers, if any, for oral use containing not more than the equivalent of 135 milligrams of propoxyphene base per dosage unit or with a concentration of not more than 2.5% in undivided preparations, being preparations whereof none of the other ingredients is a substance named or described in Schedules 1 or 2 or in Parts 1 to 5 of this schedule.

    Schedule 3 Part 5 clause 5A: substituted, on 20 December 1984, by clause 2(3) of the Misuse of Drugs Order (No 2) 1984 (SR 1984/315).

6
  • Substances containing any proportion of a substance mentioned in clause 1, clause 2, clause 3, clause 4, clause 5 or clause 5A, other than a preparation or mixture named or described in Part 6.

    Schedule 3 Part 5 clause 6: added, on 25 May 1978, by clause 2(2) of the Misuse of Drugs Order 1978 (SR 1978/143).

    Schedule 3 Part 5 clause 6: amended, on 16 December 1982, by clause 2(4) of the Misuse of Drugs Order 1982 (SR 1982/259).

Part 6

The following preparations and mixtures, namely:

  • (a) preparations containing any proportion of the following substances or of any salt of any such substance, namely, acetyldihydrocodeine, codeine, dihydrocodeine, ethylmorphine, and pholcodine when:

    • (i) compounded with 1 or more other pharmacologically active ingredients in such a way that the substance cannot be recovered by readily applicable means or in a yield which would constitute a risk to health; and

    • (ii) containing not more than 100 milligrams of the substance in each dosage unit and with a concentration of not more than 2.5% in undivided preparations:

  • (aa) preparations containing a derivative of barbituric acid named or described in Part 4 or Part 5, in solutions containing not more than 0.5% of that derivative of barbituric acid:

  • (b) preparations of cocaine containing not more than 0.1% of cocaine base, being preparations compounded with 1 or more other pharmacologically active ingredients (none of which are substances named or described in Schedules 1 or 2 or in Parts 1 to 5 of this schedule) in such a way that the preparation has no, or a negligible, risk of abuse, and in such a way that the cocaine cannot be recovered by readily applicable means or in a yield which would constitute a risk to health:

  • (c) preparations of difenoxin containing, per dosage unit, not more than 0.5 mg of difenoxin and a quantity of atropine sulphate equivalent to at least 5% of the dose of difenoxin:

  • (d) preparations of opium or morphine containing not more than 0.2% of morphine, being preparations compounded with 1 or more other pharmacologically active ingredients (none of which are substances named or described in Schedules 1 or 2 or in Parts 1 to 5 of this schedule) in such a way that the opium or the morphine, as the case may be, cannot be recovered by readily applicable means or in a yield which would constitute a risk to health:

  • (e) single dosage units of diphenoxylate containing in each unit not more than 2.5 milligrams of diphenoxylate calculated as base and not less than 25 micrograms of atropine sulphate:

  • (f) liquid preparations of diphenoxylate containing, in each millilitre, not more than 0.5 milligrams of diphenoxylate calculated as base and not less than 5 micrograms of atropine sulphate:

  • (ff) preparations of propiram containing not more than 100 mg of propiram per dosage unit and compounded with at least the same amount of methylcellulose:

  • (g) ipecacuanha and opium powder containing 10% of opium in powder and 10% of ipecacuanha root in powder intimately mixed with finely powdered lactose:

  • (h) mixtures containing not more than 1 of the preparations specified in paragraphs (a) to (g), being mixtures whereof none of the other ingredients is a substance named or described in Schedules 1 or 2 or in Parts 1 to 5 of this schedule.

    • Schedule 3 Part 6 paragraph (aa): inserted, on 25 May 1978, by clause 2(3) of the Misuse of Drugs Order 1978 (SR 1978/143).

    • Schedule 3 Part 6 paragraph (ff): inserted, on 25 May 1978, by clause 2(4) of the Misuse of Drugs Order 1978 (SR 1978/143).

Part 7

  • Schedule 3 Part 7: added, on 13 January 1988, by section 10 of the Misuse of Drugs Amendment Act (No 2) 1987 (1987 No 193).

Amphetamine analogues, in which the 1-amino-2-phenylethane nucleus carries any of the following radicals, either alone or in combination:

  • (a) 1 or 2 alkyl radicals, each with up to 6 carbon atoms, attached to the nitrogen atom:

  • (b) 1 or 2 methyl radicals, or an ethyl radical, attached to the carbon atom adjacent to the nitrogen atom:

  • (c) a hydroxy radical, attached to the carbon atom adjacent to the benzene ring:

  • (d) any combination of up to 5 alkyl radicals and/or alkoxy radicals and/or alkylamino radicals and/or alkylthio radicals (each with up to 6 carbon atoms, including cyclic radicals) and/or halogen radicals and/or nitro radicals and/or amino radicals, attached to the benzene ring.

Pethidine analogues, in which a 4-phenylpiperidine nucleus carries any of the following radicals, either alone or in combination:

  • (a) an alkyl radical, with up to 6 carbon atoms, attached to the nitrogen atom:

  • (b) a phenalkyl radical, with up to 12 carbon atoms, attached to the nitrogen atom:

  • (c) a phenalkyl radical, as in paragraph (b), with 1 or more alkyl radicals, each with up to 6 carbon atoms, attached to the benzene ring in the phenalkyl radical:

  • (d) an alkylcarbonyloxy or alkoxycarbonyl or hydroxy radical, with up to 6 carbon atoms, attached to the 4 position in the piperidine ring:

  • (e) any combination of up to 5 alkyl radicals and/or alkoxy radicals (each with up to 6 carbon atoms, including cyclic radicals) and/or halogen radicals, attached to the benzene ring.

Phencyclidine analogues, being chemical compounds with the 1-alkylamino-1-arylcyclohexane structure, with any combination of the following alkylamino and aryl radicals:

  • (a) the alkylamino radical is 1-piperidinyl, 1-pyrrolidinyl, 4-morpholinyl, or any other radical with up to 6 carbon atoms in the alkyl portion:

  • (b) the aryl radical is phenyl, thienyl, pyridinyl, or pyrrolidinyl:

  • (c) the aryl radical, as described in paragraph (b), carries any combination of up to 5 alkyl radicals and/or alkoxy radicals (each with up to 6 carbon atoms, including cyclic radicals) and/or halogen radicals.

Fentanyl analogues, in which the N-[1-(2-phenethyl)-4-piperidyl]aniline nucleus has additional radicals, either alone or in combination, attached as follows:

  • (a) an acetyl, propionyl, butenoyl or butanoyl radical, attached to the aniline nitrogen atom:

  • (b) 1 or more alkyl radicals, with up to 10 carbon atoms in total, attached to the ethyl moeity:

  • (c) any combination of up to 5 alkyl radicals and/or alkoxy radicals (each with up to 6 carbon atoms, including cyclic radicals) and/or halogen radicals, attached to each of the benzene rings.

Methaqualone analogues, in which the 3-arylquinazolin-4-one nucleus has additional radicals, either alone or in combination, attached as follows:

  • (a) an alkyl radical, with up to 6 carbon atoms, attached at the 2 position:

  • (b) any combination of up to 5 alkyl radicals and/or alkoxy radicals (each with up to 6 carbon atoms, including cyclic radicals) and/or halogen radicals, attached to each of the aryl rings.

DMT (dimethyltryptamine) analogues, in which the 3-(2-aminoethyl)indole nucleus has additional radicals, either alone or in combination, attached as follows:

  • (a) 1 or 2 alkyl radicals, each with up to 6 carbon atoms, including cyclic radicals, attached to the amino nitrogen atom:

  • (b) 1 or 2 methyl groups, or an ethyl group, attached to the carbon atom adjacent to the amino nitrogen atom:

  • (c) any combination of up to 5 alkyl radicals and/or alkoxy radicals (each with up to 6 carbon atoms, including cyclic radicals) and/or halogen radicals, attached to the benzene ring.

  • Schedule 3 Part 7 Amphetamine analogues paragraph (d): amended, on 9 August 2011, by section 9(3) of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

  • Schedule 3 Part 7 Fentanyl analogues paragraph (c): amended, on 2 September 1996, by section 8(4) of the Misuse of Drugs Amendment Act 1996 (1996 No 133).


Schedule 4
Precursor substances

s 2(1)

  • Schedule 4: added, on 12 May 1998, by section 12 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

Part 1

1 The following substances:
  • Acetic anhydride

    N-acetylanthranilic acid

    Ergometrine

    Ergotamine

    Isosafrole

    Lysergic acid

    3, 4,-methylenedioxyphenyl-2-propanone

    1-phenyl-2 propanone

    Piperonal

    Potassium permanganate

    Safrole.

    Schedule 4 Part 1 clause 1 Acetic anhydride: inserted, on 22 June 2005, by section 21(a) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Schedule 4 Part 1 clause 1 ephedrine: repealed, on 8 September 2011, by section 10 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Schedule 4 Part 1 clause 1 Potassium permanganate: inserted, on 22 June 2005, by section 21(a) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Schedule 4 Part 1 clause 1 Pseudoephedrine: repealed, on 8 September 2011, by section 10 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

2
  • The salts of the substances listed in clause 1 whenever the existence of such salts is possible.

Part 2

1 The following substances:
  • Acetone

    Anthranilic acid

    Ethyl ether

    Hydrochloric acid

    Methyl ethyl ketone

    Phenylacetic acid

    Piperidine

    Sulphuric acid

    Toluene.

    Schedule 4 Part 2 clause 1 Acetic anhydride: repealed, on 22 June 2005, by section 21(b) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Schedule 4 Part 2 clause 1 Potassium permanganate: repealed, on 22 June 2005, by section 21(b) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

2
  • The salts of the substances listed in clause 1 (other than the salts of hydrochloric acid and of sulphuric acid) whenever the existence of such salts is possible.

Part 3

  • Schedule 4 Part 3: added, on 22 June 2005, by section 20 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

1 The following substances:
  • Ephedrine

    Pseudoephedrine.

2
  • The salts of the substances listed in clause 1 whenever the existence of such salts is possible.


Schedule 5
Amount, level, or quantity at and over which controlled drugs are presumed to be for supply

ss 2(1A), 6(1)(f)

  • Schedule 5: added, on 22 June 2005, by section 22 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

1 The controlled drugs listed in the first column are presumed to be for supply at and over the amount, level, or quantity listed in the second column.
  • Amphetamine 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    Morphine 5 grams, whether or not contained in a substance, preparation, or mixture
    Cocaine half a gram, whether or not contained in a substance, preparation, or mixture
    Heroin half a gram, whether or not contained in a substance, preparation, or mixture
    Ketamine (2-(2-chlorophenyl)-2-(methylamino)-cyclohexanone) 10 grams, whether or not contained in a substance, preparation, or mixture
    Lysergide two and a half milligrams or 25 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    DOB (2-amino-1-(4-bromo-2,5-dimethoxyphenyl)propane) (also known as bromo-DMA) 100 milligrams or 25 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    MDMA (2-methylamino-1-(3,4-methylenedioxyphenyl)propane) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    N-ETHYL MDA (2-ethylamino-1-(3,4-methylenedioxyphenyl)propane) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    MDA (2-amino-1-(3,4-methylenedioxyphenyl)propane) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    Tetrahydrocannabinol (as described in Schedule 2) 250 milligrams, whether or not contained in a substance, preparation, or mixture
    Any cannabis preparation (as described in Schedule 2) 5 grams or 100 cigarettes containing the drug
    Cannabis plant (as described in Schedule 3) 28 grams or 100 cigarettes containing the drug
    BZP (1-benzylpiperazine or A2 benzylpiperazine or N-benzylpiperazine (1-benzyl-1,4-diazacyclohexane)) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    TFMPP (1-(3-trifluoromethylphenyl)piperazine or N-(3-trifluoromethylphenyl)piperazine) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    pFPP (1-(4-fluorophenyl)piperazine) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    MeOPP (1-(4-methoxyphenyl)piperazine) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    mCPP (1-(meta-chlorophenyl)piperazine) or 1-(3-chlorophenyl)piperazine) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    MBZP (1-methyl-4-benzylpiperazine) 5 grams or 100 flakes, tablets, capsules, or other drug forms each containing some quantity of the drug
    Methamphetamine 5 grams, whether or not contained in a substance, preparation, or mixture
    Ephedrine 10 grams, whether or not contained in a substance, preparation, or mixture
    Pseudoephedrine 10 grams, whether or not contained in a substance, preparation, or mixture

    Schedule 5 clause 1 Ephedrine: added, on 8 September 2011, by section 11 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Schedule 5 clause 1 Pseudoephedrine: added, on 8 September 2011, by section 11 of the Misuse of Drugs Amendment Act (No 2) 2011 (2011 No 54).

    Schedule 5 clause 1 Amphetamine: inserted, on 9  September 2005, by clause 4 of the Misuse of Drugs (Presumption of Supply—Amphetamine) Order 2005 (SR 2005/174).

    Schedule 5 clause 1 BZP: inserted, on 1 April 2008, by section 5 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

    Schedule 5 clause 1 Ketamine: inserted, on 1 December 2010, by clause 3 of the Misuse of Drugs (Presumption of Supply—Ketamine) Order 2009 (SR 2009/256)

    Schedule 5 clause 1 TFMPP: inserted, on 1 April 2008, by section 5 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

    Schedule 5 clause 1 pFPP: inserted, on 1 April 2008, by section 5 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

    Schedule 5 clause 1 MeOPP: inserted, on 1 April 2008, by section 5 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

    Schedule 5 clause 1 mCPP: inserted, on 1 April 2008, by section 5 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

    Schedule 5 clause 1 MBZP: inserted, on 1 April 2008, by section 5 of the Misuse of Drugs (Classification of BZP) Amendment Act 2008 (2008 No 5).

2
  • Any controlled drug not specified in clause 1 is presumed to be for supply at and over the level of 56 grams.


Misuse of Drugs Amendment Act 1978

Public Act1978 No 65
Date of assent16 October 1978
Commencement16 October 1978
1 Short Title
  • This Act may be cited as the Misuse of Drugs Amendment Act 1978, and shall be read together with and deemed part of the Misuse of Drugs Act 1975 (hereinafter referred to as the principal Act).

Part 2
Special provisions relating to detection, enforcement, and sentencing

10 Interpretation
  • (1) In this Part, unless the context otherwise requires,—

    dealing in cannabis on a substantial scale means—

    • (a) dealing (in any of the ways referred to in section 6(1) of the principal Act) with a substantial amount of a controlled drug in respect of which a prescribed cannabis offence may be committed:

    • (b) cultivation of a prohibited plant (being a prohibited plant in respect of which a prescribed cannabis offence may be committed) on a substantial scale

    drug dealing offence means,—

    • (b) any offence against section 6 of the principal Act—

    in relation to a Class A controlled drug or a Class B controlled drug

    emergency permit means a permit granted under section 19 to intercept a private communication by means of an interception device

    facility means an electronic address, phone number, or similar facility that enables private communications to—

    • (a) take place between individuals; or

    • (b) be sent to or from an identified individual

    intercept, in relation to a private communication, includes hear, listen to, record, monitor, acquire, or receive the communication either—

    • (a) while it is taking place; or

    • (b) while it is in transit

    interception device

    • (a) means any electronic, mechanical, or electromagnetic instrument, apparatus, equipment, or other device that is used or is capable of being used to intercept a private communication; but

    • (b) does not include a hearing aid or similar device used to correct subnormal hearing of the user to no better than normal hearing

    interception warrant means a warrant granted under section 15 or section 15B to intercept a private communication by means of an interception device

    organised criminal enterprise means a continuing association of 3 or more persons having as its object or as one of its objects the acquisition of substantial income or assets by means of a continuing course of criminal conduct

    prescribed cannabis offence means an offence against—

    • (a) section 6 of the principal Act in relation to a Class C controlled drug specified or described in Part 1 of Schedule 3 of the principal Act (other than catha edulis plant or coca leaf); or

    • (b) section 9 of the principal Act in relation to a prohibited plant of the genus Cannabis

    private communication

    • (a) means a communication (whether in oral or written form or otherwise) made under circumstances that may reasonably be taken to indicate that any party to the communication desires it to be confined to the parties to the communication; but

    • (b) does not include such a communication occurring in circumstances in which any party ought reasonably to expect that the communication may be intercepted by some other person not having the express or implied consent of any party to do so

    tracking device means a device capable of transmitting a signal to a receiver for the purpose of indicating the location of the device.

    (2) A reference in this Part to a party to a private communication is a reference to—

    • (a) any originator of the communication and any person intended by the originator to receive it; and

    • (b) a person who, with the express or implied consent of any originator of the communication or any person intended by the originator to receive it, intercepts the communication.

    (3) For the purposes of section 12,—

    craft, goods, package, and vehicle have the same meanings as in section 2(1) of the Customs and Excise Act 1996.

    Section 10(1) dealing in cannabis on a substantial scale: inserted, on 1 February 1998, by section 3(2) of the Misuse of Drugs Amendment Act (No 2) 1997 (1997 No 96).

    Section 10(1) drug dealing offence: substituted, on 12 May 1998, by section 13 of the Misuse of Drugs Amendment Act 1998 (1998 No 14).

    Section 10(1) emergency permit: amended, on 1 October 2003, by section 35 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 10(1) facility: inserted, on 1 October 2003, by section 35 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 10(1) intercept: substituted, on 1 October 2003, by section 35 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 10(1) interception device: inserted, on 1 October 2003, by section 35 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 10(1) interception warrant: amended, on 1 October 2003, by section 35 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 10(1) interception warrant: amended, on 1 February 1998, by section 3(1) of the Misuse of Drugs Amendment Act (No 2) 1997 (1997 No 96).

    Section 10(1) listening device: repealed, on 1 October 2003, by section 35 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 10(1) organised criminal enterprise: inserted, on 1 February 1998, by section 3(2) of the Misuse of Drugs Amendment Act (No 2) 1997 (1997 No 96).

    Section 10(1) prescribed cannabis offence: inserted, on 1 February 1998, by section 3(2) of the Misuse of Drugs Amendment Act (No 2) 1997 (1997 No 96).

    Section 10(1) private communication: substituted, on 1 October 2003, by section 35 of the Crimes Amendment Act 2003 (2003 No 39).

    Section 10(1) proper officer of Customs: repealed, on 1 October 1996, by section 289(1) of the Customs and Excise Act 1996 (1996 No 27).

    Section 10(3): substituted, on 1 October 1996, by section 289(1) of the Customs and Excise Act 1996 (1996 No 27).

    Section 10(3): amended, on 31 October 2003, by section 3(2) of the Misuse of Drugs Amendment Act (No 2) 2003 (2003 No 107).

    Section 10(3) postal article: repealed, on 1 April 1998, by section 62(1) of the Postal Services Act 1998 (1998 No 2).

11 Application of Part

Special powers of Police and Customs officers

12 Allowing delivery of unlawfully imported drugs or precursor substances for purpose of detection, etc
  • (1) Where any Customs officer acting in the course of his or her official duties believes on reasonable grounds that there is in or on any craft, package, mail, vehicle, or goods any controlled drug or precursor substance that has been imported into New Zealand in contravention of section 6(1)(a) or section 12AB of the principal Act, he or she may, for the purpose of his or her investigation of the matter, leave or replace that drug or precursor substance, or any portion of it, in or on the craft, package, mail, vehicle, or goods and may, in the same manner as if there had been delivery from Customs control,—

    • (a) allow the craft or vehicle to leave; or

    • (b) allow the package or goods to be collected by or delivered to or on behalf of the consignee; or

    • (c) return the goods or mail to the appropriate carrier for delivery to the addressee—

    as the case may require.

    (2) No Customs officer who exercises any power conferred by subsection (1), and no officer or employee of any carrier who, in the course of his or her duties, does anything in respect of any goods or mail returned to a carrier in accordance with that subsection (whether or not he or she knows that the goods or mail contains a controlled drug or precursor substance), is under any criminal or civil liability in respect of the exercise of that power or, as the case requires, the doing of that thing.

    Section 12: substituted, on 1 October 1996, by section 289(1) of the Customs and Excise Act 1996 (1996 No 27).

    Section 12 heading: amended, on 22 June 2005, by section 24(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12(1): amended, on 22 June 2005, by section 24(2)(a) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12(1): amended, on 22 June 2005, by section 24(2)(b) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12(1): amended, on 22 June 2005, by section 24(2)(c) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12(1): amended, on 1 April 1998, by section 62(1) of the Postal Services Act 1998 (1998 No 2).

    Section 12(1)(c): substituted, on 1 April 1998, by section 62(1) of the Postal Services Act 1998 (1998 No 2).

    Section 12(2): substituted, on 1 April 1998, by section 62(1) of the Postal Services Act 1998 (1998 No 2).

    Section 12(2): amended, on 22 June 2005, by section 24(3) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

12A Searches relating to persons involved in delivery under section 12
  • (1) If the circumstances in subsection (2) exist, a constable or a Customs officer may, during the course of a delivery in relation to which a Customs officer has exercised his or her powers under section 12,—

    • (a) search any person involved in that delivery; and

    • (b) detain that person for the purpose of carrying out that search.

    (2) The circumstances are that the constable or the Customs officer believes on reasonable grounds that the person is in possession of any of the following:

    • (a) a controlled drug:

    • (b) a precursor substance:

    • (c) a package in relation to which the Customs officer has replaced all or a portion of any controlled drug or precursor substance:

    (3) Reasonable force may be used, if necessary, for either or both of the following purposes:

    • (a) to search a person under subsection (1):

    • (b) to detain a person under subsection (1).

    (4) A constable or a Customs officer may, without a search warrant issued under section 198 of the Summary Proceedings Act 1957, enter any building, craft, carriage, vehicle, premises, or place in order to carry out a search under subsection (1).

    (5) A constable or a Customs officer who undertakes a search under subsection (1) must, within 3 working days of the search, give a written report of the search, the circumstances in which the search was conducted, and the matters that gave rise to the reasonable grounds to believe required under subsection (2), to—

    • (a) in the case of a constable, the Commissioner of Police; and

    • (b) in the case of a Customs officer, the Chief Executive of the New Zealand Customs Service.

    Section 12A: inserted, on 22 June 2005, by section 25 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12A(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 12A(2): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 12A(4): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 12A(5): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 12A(5)(a): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

12B Seizure of items found during search under section 12A
  • (1) A constable or a Customs officer may seize any thing found on or about a person when carrying out a search under section 12A(1) that the constable or the Customs officer has reasonable cause to suspect is a thing described in any of paragraphs (a) to (d) of section 12A(2).

    (2) Reasonable force may be used, if necessary, to seize the thing.

    Section 12B: inserted, on 22 June 2005, by section 25 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12B(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

12C Obligations on constable or Customs officer conducting search under section 12A to identify self and power relied on
  • (1) Every constable or Customs officer who exercises a power of search under section 12A(1) must—

    • (a) identify himself or herself to any person he or she intends to search; and

    • (b) advise that person that the search is being undertaken under the authority of section 12A(1).

    (2) Every constable or Customs officer who enters any building, craft, carriage, vehicle, premises, or place in order to carry out a search under section 12A(1) must—

    • (a) identify himself or herself to any person who questions his or her right to enter; and

    • (b) advise that person that the entry is being undertaken under the authority of section 12A(1).

    Section 12C: inserted, on 22 June 2005, by section 25 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12C heading: amended, on 1 October 2008, pursuant to section 116(a)(i) of the Policing Act 2008 (2008 No 72).

    Section 12C(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 12C(2): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

12D International controlled delivery and liability for offences
  • (1) In this section, an international controlled delivery means allowing a controlled drug or precursor substance (or substance substituted in the place of a controlled drug or precursor substance) to pass through or into the territory of 1 or more countries—

    • (a) with the agreement of the relevant law enforcement agencies of the countries which it is to pass through or into; and

    • (b) with a view to identifying persons involved in the commission of an offence—

      • (ii) that would, if done or committed in New Zealand, be an offence under either of those sections.

    (2) Nothing in subsection (3) affects the liability of any person charged with an offence under section 6(1)(a) or section 12AB or section 12AC of the principal Act.

    (3) Any constable, Customs officer, or officer of a relevant law enforcement agency with which there is an agreement under subsection (1)(a) who is involved in an international controlled delivery—

    • (a) does not commit an offence under section 6(1)(a), 12AB, or 12AC of the principal Act by reason of taking part in that international controlled delivery; and

    • (b) unless he or she is acting in bad faith, is not subject to any criminal or civil liability as a result of taking part in that international controlled delivery.

    Section 12D: inserted, on 22 June 2005, by section 25 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 12D(3): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

Internal concealment

  • Heading: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

13A Power to detain on belief of internal concealment
  • (1) If any constable or officer of Customs has reasonable cause to believe that any person has any Class A controlled drug or Class B controlled drug secreted within that person’s body for any unlawful purpose, the constable or officer of Customs may cause that person to be detained under this section.

    (2) For the purposes of subsection (1), a person has any Class A controlled drug or Class B controlled drug secreted within that person’s body if—

    • (a) the drug is within any of that person’s body cavities; or

    • (b) that person has swallowed the drug in such a manner that it may pass through the body, or be regurgitated, intact, but the drug is still within the body at the material time.

    (3) In subsection (1), unlawful purpose means the commission of an offence against the principal Act, and the concealment of the commission of any such offence.

    Section 13A: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

    Section 13A(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

13B Duties of officer in ordering detention
  • On causing any person to be detained under section 13A, a constable or an officer of Customs shall as soon as possible, unless the detention sooner ceases in accordance with paragraph (a) or paragraph (b) or paragraph (c) of section 13H,—

    • (a) inform the detained person of the reason for the detention, in words sufficient to give the detained person notice of the true reason for the detention; and

    • (b) hand to the detained person a statement of rights in the form set out in Schedule 2; and

    • (c) arrange for the attendance of a medical practitioner (who shall be nominated or approved for the purpose by the Commissioner of Police or the Chief Executive of the New Zealand Customs Service, either generally or in any particular case or class of case), and, in the presence of that medical practitioner, ask the detained person if he or she wishes to undergo an examination of 1 or more of the kinds specified in section 13C(1); and

    • (d) apply to a District Court Judge, in accordance with section 13E, for a warrant authorising the continued detention of the detained person under section 13A.

    Section 13B: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

    Section 13B: amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13B(c): amended, on 1 October 1996, by section 289(1) of the Customs and Excise Act 1996 (1996 No 27).

13C Internal examination of detained person
  • (1) The kinds of examination that a person who is detained under section 13A may undergo are as follows:

    • (a) a physical examination (whether or not facilitated by an instrument or device) to be conducted by a medical practitioner nominated or approved for the purpose by the Commissioner of Police or the Chief Executive of the New Zealand Customs Service, either generally or in any particular case or class of case:

    • (b) an X-ray examination with or without a contrast agent:

    • (c) an ultrasound scan.

    (2) Except in a case where the detained person immediately makes it clear that he or she does not wish to undergo any examination, the medical practitioner called under section 13B(c) shall explain to the detained person what is involved in each kind of examination.

    (3) If the detained person wishes to undergo an examination of a kind described in subsection (1), the detained person shall sign a written statement to the effect that he or she consents to the examination, and the medical practitioner shall endorse on the written consent a certificate to the effect that the medical practitioner has advised the detained person of what is involved in the examination and is satisfied that the detained person, when giving consent, understood what is involved in that examination.

    (4) Notwithstanding that any such detained person states that he or she does not wish to undergo any examination of a kind described in subsection (1), the detained person may subsequently, at any time while the detention is continuing, advise any constable or officer of Customs that he or she now wishes to undergo such an examination, in which case the provisions of subsections (2) and (3) shall apply with any necessary modifications.

    (5) As soon as practicable after any such detained person has consented to undergo any such examination, a constable or an officer of Customs shall make all necessary arrangements for that examination to take place.

    (6) Notwithstanding any of the foregoing provisions of this section, no such detained person shall be entitled to insist on undergoing an examination of a particular kind if the necessary equipment is not reasonably available for the purpose.

    (7) Nothing in the foregoing provisions of this section shall preclude the detained person from requesting or consenting to the administration to him or her of a laxative or any other similar substance; and, where the detained person makes any such request or gives any such consent, a constable or an officer of Customs shall record the particulars of the case, and those particulars shall be supplied to the Judge whenever an application for the grant or renewal of a detention warrant is made.

    Section 13C: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

    Section 13C(1)(a): amended, on 1 October 1996, by section 289(1) of the Customs and Excise Act 1996 (1996 No 27).

    Section 13C(4): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13C(5): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13C(7): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

13D Certificate by person conducting examination
  • (1) The medical practitioner or other person who conducts an examination of any person detained under section 13A shall, on concluding the examination, certify the results of the examination in whichever of the following forms is appropriate:

    • (a) that, in his or her professional judgment, the detained person has nothing secreted within that person’s body, or within that part of the body to which the examination related, that could be or contain a Class A controlled drug or a Class B controlled drug:

    • (b) that, in his or her professional judgment, the detained person has something secreted within that person’s body that could be or contain a Class A controlled drug or a Class B controlled drug:

    • (c) that the results of the examination are inconclusive.

    (2) A copy of every certificate given under subsection (1) shall be given to—

    • (a) the detained person; and

    • (b) the barrister or solicitor appointed under section 13F; and

    • (c) the medical practitioner appointed under that section.

    Section 13D: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

13E Detention warrant
  • (1) Subject to subsection (2), every application for a warrant authorising the continued detention of any person under section 13A shall be made by a constable or an officer of Customs in writing and on oath, and shall set out, or be accompanied by, the following particulars:

    • (a) the facts relied upon to show that there is reasonable cause to believe that the detained person has any Class A controlled drug or Class B controlled drug secreted within that person’s body for any unlawful purpose:

    • (b) the time at which, the date on which, and the place at which the detention commenced under section 13A:

    • (c) the address, and a description of the nature, of the premises in which the detained person is being detained, and, if it is proposed that the detained person be moved to any other premises for the purposes of the detention, the address, and a description of the nature, of those other premises:

    • (d) the time or times at which, and the date or dates on which, the detained person was asked if he or she wished to undergo any examination of a kind described in section 13C(1), and the detained person’s response to any such question, including the reasons given by the detained person for any negative response:

    • (e) if any such examination has been conducted, the results of that examination as set out in the certificate given under section 13D(1).

    (2) In any case where, because of the urgency of the matter or for any other sufficient cause, it seems proper to do so, a District Court Judge may permit an application under this section to be made on oath orally, but in that event the Judge shall make a note in writing of the particulars referred to in paragraphs (a) to (e) of subsection (1).

    (3) In considering an application made under this section, the Judge may take into account any oral or documentary material that the Judge considers relevant, whether or not it would be admissible in a court of law.

    (4) If, on an application made under this section, a Judge is satisfied—

    • (a) that there has been reasonable compliance with the requirements of section 13B; and

    • (b) that there is reasonable cause to believe that the detained person has secreted within that person’s body any Class A controlled drug or Class B controlled drug for any unlawful purpose; and

    • (c) that the premises in which the detained person is being detained, or any other premises in which it is proposed to detain that person, are suitable for the purpose,—

    the Judge may grant a detention warrant in the prescribed form authorising the continued detention of the person to whom it relates under section 13A.

    (5) A detention warrant issued under subsection (4) shall authorise the continued detention of the person named in it in the premises specified in it until—

    • (a) the expiry of the period of 7 days commencing with the date on which the detention under section 13A commenced, or such shorter period as the Judge may specify in the warrant; or

    • (b) the detention is sooner brought to an end in any of the circumstances described in section 13H.

    (6) On granting a detention warrant under this section, a Judge—

    • (a) shall record in writing his or her reasons for granting the warrant; and

    • (b) may impose all such conditions relating to the circumstances and conduct of the detention as the Judge thinks fit.

    Section 13E: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

    Section 13E(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

13EA Searches associated with detention warrant
  • (1) If the circumstances in subsection (2) exist, a constable or a Customs officer may undertake any of the following in relation to a person (person A):

    • (c) both a rub-down search and a strip search.

    (2) The circumstances are that—

    • (a) a detention warrant has been issued under section 13E in relation to person A; and

    • (b) the constable or the Customs officer has reasonable cause to suspect that person A has hidden on or about his or her person any Class A controlled drug or Class B controlled drug.

    (3) In deciding what type of search to undertake under subsection (1), a constable or a Customs officer must have regard to all of the relevant circumstances, including, without limitation, the matters referred to in section 13ED(2).

    (4) If, as a result of a search under subsection (1), a constable or a Customs officer finds any Class A controlled drug or Class B controlled drug, he or she may take possession of it.

    (5) Reasonable force may be used, if necessary, to undertake a search under subsection (1).

    (6) If a person who is undergoing a search under subsection (1) makes a request for an internal examination under section 13C(4), the constable or the Customs officer conducting the search may continue with and complete the search before arranging for the internal examination to take place.

    Section 13EA: inserted, on 22 June 2005, by section 26 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 13EA(1): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13EA(2)(b): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13EA(3): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13EA(4): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13EA(6): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

13EB Definition of rub-down search
  • (1) For the purposes of this section, section 13EA and sections 13ED to 13M, a rub-down search means a search of a clothed person in which the person conducting the search may do all or any of the following:

    • (a) run or pat his or her hand over the body of the person being searched, whether outside or inside the clothing (other than any underclothing) of that person:

    • (b) insert his or her hand inside any pocket or pouch in the clothing (other than any underclothing) of the person being searched:

    • (c) for the purpose of permitting a visual inspection, require the person being searched to do all or any of the following:

      • (i) open his or her mouth:

      • (ii) display the palms of his or her hands:

      • (iii) display the soles of his or her feet:

      • (iv) lift or rub his or her hair.

    (2) For the purpose of facilitating any of the actions referred to in any of paragraphs (a) to (c) of subsection (1), the person conducting a rub-down search may require the person being searched—

    • (a) to remove, raise, lower, or open any outer clothing (including (without limitation) any coat, jacket, jumper, or cardigan) being worn by the person being searched, except where that person has no other clothing, or only underclothing, under that outer clothing; and

    • (b) to remove any head covering, gloves, or footwear (including socks or stockings) being worn by that person.

    (3) Authority to conduct a rub-down search includes the authority to conduct a visual examination (whether or not facilitated by any instrument or device designed to illuminate or magnify) of the mouth, nose, and ears, but does not authorise the insertion of any instrument, device, or thing into any such orifice.

    (4) Authority to conduct a rub-down search of a person includes the authority to search—

    • (a) any item carried by, or in the possession of, the person; and

    • (b) any outer clothing removed, raised, lowered, or opened for the purposes of the search; and

    • (c) any head covering, gloves, or footwear (including socks or stockings) removed for the purposes of the search.

    Section 13EB: inserted, on 22 June 2005, by section 26 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

13EC Definition of strip search
  • (1) For the purposes of this section, section 13EA, and sections 13ED to 13M, a strip search means a search where the person conducting the search may require the person being searched to remove, raise, lower, or open all or any of that latter person’s clothing.

    (2) For the purpose of facilitating a strip search, the person conducting the search may require the person being searched to do all or any of the following:

    • (a) open his or her mouth:

    • (b) display the palms of his or her hands:

    • (c) lift or rub his or her hair:

    • (d) display the soles of his or her feet:

    • (e) raise his or her arms to expose his or her armpits:

    • (f) with his or her legs spread apart, bend his or her knees.

    (3) Authority to conduct a strip search includes the authority to conduct a visual examination (whether or not facilitated by any instrument or device designed to illuminate or magnify) of the mouth, nose, and ears, but does not authorise the insertion of any instrument, device, or thing into any such orifice.

    (4) Authority to conduct a strip search of a person includes the authority to search—

    • (a) any item of clothing removed, raised, lowered, or opened for the purposes of the search; and

    • (b) any item carried by, or in the possession of, the person.

    Section 13EC: inserted, on 22 June 2005, by section 26 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

13ED Restrictions on searches associated with detention warrant
  • (1) A rub-down search or strip search, or both, may be carried out only by a person of the same sex as the person to be searched, and no strip search may be carried out in view of any person who is not of the same sex as the person to be searched.

    (2) A person who carries out a rub-down search or strip search, or both, must conduct the search with decency and sensitivity and in a manner that affords to the person being searched the greatest degree of privacy and dignity consistent with the purpose of the search.

    (3) No constable or Customs officer may conduct a strip search unless another constable or officer is also present.

    (4) A strip search of a person must not be carried out in view of any other person who is detained or being searched.

    Section 13ED: inserted, on 22 June 2005, by section 26 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 13ED(3): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

13EE Reporting search associated with detention warrant
  • A constable or a Customs officer who undertakes a search under section 13EA must, within 3 working days of the search, give a written report of the search, the circumstances in which it was conducted, and the matters that gave rise to the reasonable cause to suspect required by section 13EA(2)(b) to,—

    • (a) in the case of a constable, the Commissioner of Police; and

    • (b) in the case of a Customs officer, the Chief Executive of the New Zealand Customs Service.

    Section 13EE: inserted, on 22 June 2005, by section 26 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 13EE: amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13EE(a): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

13F On grant of warrant, Judge to appoint barrister or solicitor and medical practitioner
  • (1) On granting a detention warrant under section 13E, a District Court Judge shall appoint, or arrange for the appointment of, a barrister or solicitor and a medical practitioner to report to the court on the matters referred to in subsections (2) and (3).

    (2) The function of the barrister or solicitor appointed under this section shall be to satisfy himself or herself—

    • (a) that the detention is being conducted in accordance with the provisions of this Act, the terms of the detention warrant, and any directions given by the Judge; and

    • (b) that the detained person is aware of his or her rights in relation to the detention, and that the exercise of any of those rights by that person is not being interfered with unreasonably,—

    and to report to the Judge if the barrister or solicitor is not so satisfied in any particular respect.

    (3) The function of the medical practitioner appointed under this section shall be to satisfy himself or herself—

    • (a) that the detained person is being accommodated, fed, and generally cared for in a reasonable and proper manner; and

    • (b) that the detained person is being offered all such medical care (if any) as may seem to the medical practitioner to be necessary or desirable in the interests of that person,—

    and to report to the Judge if the medical practitioner is not so satisfied in any particular respect.

    (4) Notwithstanding anything in subsection (2) or subsection (3), where—

    • (a) the detained person consults a barrister or solicitor of that person’s choosing and that barrister or solicitor agrees to act for that person, the barrister or solicitor appointed under subsection (1) shall not be responsible for any matter falling within the normal responsibilities of a barrister or solicitor acting for a client; or

    • (b) the detained person consults a medical practitioner of that person’s choosing and that medical practitioner agrees to attend that person as a patient, the medical practitioner appointed under subsection (1) shall not be responsible for any matter falling within the normal responsibilities of a medical practitioner attending a patient.

    (5) On appointing a barrister or solicitor or a medical practitioner under this section, or at any time thereafter while the detention continues, a District Court Judge may give to the barrister or solicitor or medical practitioner all such directions relating to the functions of the barrister or solicitor or medical practitioner as the Judge thinks fit.

    Section 13F: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

13G Rights of access to person in detention
  • (1) The following persons shall at all times have the right of access to any person who is being detained under section 13A:

    • (a) the barrister or solicitor appointed under section 13F:

    • (b) the medical practitioner appointed under that section.

    (2) The following persons shall at all reasonable times have the right of access to any person who is being detained under section 13A:

    • (a) any barrister or solicitor who is acting for the detained person:

    • (b) any medical practitioner who is attending the detained person as a patient:

    • (c) any other person whom the detained person reasonably wishes to see.

    (3) Nothing in subsection (2), or any other enactment or rule of law, shall entitle any person to have access to the detained person—

    • (a) in the absence of any constable or officer of Customs who is for the time being guarding the detained person; or

    • (b) otherwise than subject to such reasonable conditions as may be necessary to ensure the safety of the detained person or to avoid the frustration of the purpose of the detention.

    Section 13G: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

    Section 13G(3)(a): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

13H Expiry of detention
  • The detention of any person under section 13A shall cease in each of the following circumstances:

    • (a) where the detained person is arrested:

    • (b) where a certificate is given under section 13D, following an examination, to the effect that, in the professional judgment of the person conducting the examination, the detained person has nothing secreted within that person’s body that could be or contain a Class A controlled drug or a Class B controlled drug:

    • (c) where the constable or officer of Customs who is in charge of the case forms the view that there is no longer reasonable cause to believe that the detained person has any Class A controlled drug or Class B controlled drug secreted within that person’s body for any unlawful purpose:

    • (d) where an application to a District Court Judge for a detention warrant, or for the renewal of a detention warrant, in respect of the detained person is declined:

    • (e) where the warrant is cancelled on appeal under section 13L.

    Section 13H: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

    Section 13H(c): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

13I Renewal of warrants
  • (1) Any District Court Judge may from time to time grant a renewal of a detention warrant upon application made at any time before the warrant (or any current renewal of the warrant) has expired.

    (2) Every application for renewal of a detention warrant shall be made by a constable or an officer of Customs in writing and on oath, and shall set out, or be accompanied by, the following particulars:

    • (a) the facts relied upon to show that there is still reasonable cause to believe that the detained person has any Class A controlled drug or Class B controlled drug secreted within that person’s body for any unlawful purpose:

    • (b) the date or dates on which the detained person was asked to consent to undergo any examination of a kind described in section 13C, and the detained person’s response to that request, including any reasons given by the detained person for any negative response:

    • (c) if any such examination has been conducted, the results of that examination as set out in the certificate given under section 13D(1):

    • (ca) the date or dates of any rub-down search or strip search undertaken under section 13EA, the circumstances in which it was conducted, and the results of the search:

    • (d) any matters that the barrister or solicitor appointed under section 13F wishes to draw to the attention of the Judge who is to consider the application for renewal:

    • (e) any matters that the medical practitioner appointed under that section wishes to draw to the attention of that Judge:

    • (f) any matters that any barrister or solicitor who is acting for the detained person, or any medical practitioner who is attending the detained person as a patient, wishes to draw to the attention of that Judge.

    (3) Every such application shall be supported by such other information as the Judge may require.

    (4) Notice of every such application shall be given to the barrister or solicitor appointed under section 13F and to any barrister or solicitor who is acting for the detained person.

    (5) Notwithstanding any of the preceding provisions of this section or any enactment or rule of law to the contrary, neither the detained person nor any person referred to in any of paragraphs (d) to (f) of subsection (2) shall be entitled to see or hear any evidence that was adduced in support of the original application for the grant of the detention warrant, or any evidence adduced in support of the application for the renewal of the warrant and relating to any matter other than one to which paragraph (b) or paragraph (c) or paragraph (ca) of that subsection applies; and for the purposes of this subsection, every such person shall be excluded from the hearing while any such evidence is being given.

    (6) In considering an application made under this section, the Judge may take into account any oral or documentary material that the Judge considers relevant, whether or not it would be admissible in a court of law.

    (7) Without limiting subsection (3), before determining an application for the renewal of a detention warrant under this section, a District Court Judge may—

    • (a) call for a report from the barrister or solicitor referred to in paragraph (d) of subsection (2), or from the medical practitioner referred to in paragraph (e) of that subsection, on any matter relating to the detention or to the application for the renewal of the detention warrant; and

    • (b) hear any person referred to in any of paragraphs (d) to (f) of that subsection in respect of the application.

    (8) A renewal of a detention warrant may be granted under this section if the Judge is satisfied that the circumstances described in section 13A still obtain.

    (9) Every renewal of a detention warrant shall be valid for a period of 7 days commencing with the date on which it is granted, or such shorter period as the Judge may specify in the renewal.

    (10) Where an application for the renewal of a detention warrant is duly made before the expiration of the warrant (or of any current renewal of the warrant), the warrant shall continue in force until the application is determined notwithstanding the expiration of the period for which the warrant was issued or last renewed.

    (11) Nothing in this section shall prevent a Judge from granting a second or subsequent renewal of a detention warrant upon an application duly made under this section:

    provided that no detention under section 13A shall continue for longer than 21 days.

    (12) On granting a renewal of a detention warrant under this section, a Judge—

    • (a) shall record in writing his or her reasons for granting the renewal; and

    • (b) may impose all such conditions relating to the circumstances and conduct of the detention as the Judge thinks fit.

    Section 13I: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

    Section 13I(2): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13I(2)(ca): inserted, on 22 June 2005, by section 27(1) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 13I(5): amended, on 22 June 2005, by section 27(2) of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

13J Powers of officers of Customs
  • The powers conferred by sections 13A to 13I may be exercised by any officer of Customs only in respect of offences against the principal Act involving the importation into or the exportation from New Zealand of any Class A controlled drug or Class B controlled drug.

    Section 13J: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

13K Inadmissibility of certain confessions or admissions by detained person
  • (1) Where any person who is being detained under section 13A makes any confession or admission in respect of any offence other than a relevant offence, no evidence of that confession or admission, or of its substance, meaning, or purport, shall be given in any court.

    (2) For the purposes of this section, a relevant offence is one with which the detained person may be liable to be charged by virtue of having any controlled drug secreted within that person’s body at any time during the detention.

    Section 13K: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

13L Appeal against grant or renewal of detention warrant, etc
  • (1) Where a District Court Judge grants a detention warrant under section 13E, or grants a renewal of a detention warrant under section 13I, or imposes any condition under either of those sections relating to the circumstances or conduct of the detention, the detained person may appeal to the High Court against that decision.

    (2) Where a notice of appeal is filed in the High Court under this section, the Registrar of the court in which the decision under appeal was made shall forward the court file to the High Court.

    (3) The fact that an appeal is lodged or is pending under this section shall not affect the detention, which, subject to section 13H, shall continue pending the determination of the appeal.

    (4) The detained person shall not have the right to attend or be heard personally in respect of the appeal, but may be represented by counsel.

    (5) Notwithstanding any of the provisions of this section or any enactment or rule of law to the contrary, neither the detained person nor his or her counsel shall be entitled to see or hear any evidence that was adduced in support of the original application for the grant of the detention warrant, or any evidence adduced in opposition to the appeal and relating to any matter other than one referred to in paragraph (b) or paragraph (c) of section 13I(2); and for the purposes of this subsection, any counsel representing the detained person shall be excluded from the hearing while any such evidence is being given.

    (6) Every appeal under this section shall be by way of rehearing.

    (7) On hearing any such appeal, the High Court may take into account any oral or documentary material that the court considers relevant, whether or not it would otherwise be admissible.

    (8) Without limiting subsection (7), before determining an appeal under this section, the court may—

    • (a) call for a report from the barrister or solicitor or the medical practitioner appointed under section 13F on any matter relating to the detention or to the appeal; and

    • (b) hear any such barrister or solicitor or medical practitioner, or any other medical practitioner who is attending the detained person as a patient.

    (9) On hearing any appeal under this section, the High Court may confirm, reverse, or modify the decision under appeal.

    (10) Where the High Court reverses the decision to grant a detention warrant or the renewal of a detention warrant, it shall cancel the warrant.

    (11) The decision of the High Court on an appeal under this section shall be final.

    Section 13L: inserted, on 1 October 1985, by section 2 of the Misuse of Drugs Amendment Act 1985 (1985 No 130).

13M Commissioner of Police and Chief Executive of New Zealand Customs Service to report to Parliament
  • The Commissioner of Police shall include in every annual report prepared by the Commissioner for the purposes of section 101 of the Policing Act 2008, and the Chief Executive of the New Zealand Customs Service shall include in every annual report prepared by the Chief Executive for submission to Parliament, the following information in respect of the period under review:

    • (a) the number of applications for detention warrants made under section 13E by any constable or (as the case may require) any officer of Customs:

    • (b) the number of applications for renewals of detention warrants made under section 13I by any constable or (as the case may require) any officer of Customs:

    • (c) the number of such applications referred to in each of the preceding paragraphs of this section that were granted and the number that were refused:

    • (d) the average duration of the detention warrants (including renewals) granted on applications by constables or (as the case may require) officers of Customs:

    • (e) the number of prosecutions that have been instituted in which has been adduced evidence obtained directly during the detention of any persons pursuant to detention warrants granted on applications by constables or (as the case may require) officers of Customs, and the results of those prosecutions.

    • (f) the number of rub-down searches and strip searches undertaken by constables or Customs officers under section 13EA.

    Section 13M: substituted, on 1 October 1996, by section 289(1) of the Customs and Excise Act 1996 (1996 No 27).

    Section 13M: amended, on 1 October 2008, by section 130(1) of the Policing Act 2008 (2008 No 72).

    Section 13M(a): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13M(b): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13M(d): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13M(e): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

    Section 13M(f): added, on 22 June 2005, by section 28 of the Misuse of Drugs Amendment Act 2005 (2005 No 81).

    Section 13M(f): amended, on 1 October 2008, pursuant to section 116(a)(ii) of the Policing Act 2008 (2008 No 72).

Applications for interception warrants in relation to drug dealing offences

  • Heading: substituted, on 1 February 1998, by section 4 of the Misuse of Drugs Amendment Act (No 2) 1997 (1997 No 96).

14 Application by Police for warrant to intercept private communications
  • (1) An application may be made in accordance with this section to a Judge of the High Court for a warrant for any constable to intercept a private communication by means of an interception device in any case where there are reasonable grounds for believing that—

    • (a) a person has committed, or is committing, or is about to commit, a drug dealing offence; and

    • (b) it is unlikely that the Police investigation of the case could be brought to a successful conclusion without the grant of such a warrant.

    (2) Every application under subsection (1) shall be made by a constable who is of or above the level of position of inspector, in writing, and on oath, and shall set out the following particulars:

    • (a) the facts relied upon to show that there are reasonable grounds for believing that a person has committed, or is committing, or is about to commit, a drug dealing offence; and

    • (b) a description of the manner in which it is proposed to intercept private communications; and

    • (c) the name and address, if known, of the suspect whose private communications there are reasonable grounds for believing will assist the Police investigation of the case or, if the name and address of the suspect are not known, a general description of the premises, place, thing, or type of facility in respect of which it is proposed to intercept private communications, being premises or a place, thing, or type of facility believed to be used for any purpose by any person involved in the drug dealing offence; and

    • (d)