- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (23/12/2009)
- Gwreiddiol (Fel y'i Deddfwyd)
Version Superseded: 16/04/2010
Point in time view as at 23/12/2009.
There are currently no known outstanding effects for the Misuse of Drugs Act 1971, Part II.
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
1U.K.The following substances and products, namely:—
[F1(a)]
Acetyldihydrocodeine.
Amphetamine.
[F2Cannabinol]
[F2Cannabinol derivatives]
[F2Cannabis and cannabis resin]
F3...
Codeine.
F4. . .
Dihydrocodeine.
Ethylmorphine (3-ethylmorphine).
[F5Glutethimide.]
[F5Lefetamine.]
[F6Mecloqualone.]
[F6Methaqualone.]
[F7Methcathinone]
F8...
[F9a-Methylphenethylhydroxylamine]
Methylphenidate.
[F6Methylphenobarbitone.]
Nicocodine.
[F10Nicodicodine (6-nicotinoyldihydrocodeine).]
Norcodeine.
[F11Pentazocine.]
Phenmetrazine.
Pholcodine.
[F12Propiram.]
[F7Zipeprol]
[F1(b)any 5,5 disubstituted barbituric acid.]
[F13(c)[2,3–Dihydro–5–methyl–3–(4–morpholinylmethyl)pyrrolo[1, 2, 3–de]–1,4–benzoxazin–6–yl]–1–naphthalenylmethanone.
3–Dimethylheptyl–11–hydroxyhexahydrocannabinol.
[9–Hydroxy–6–methyl–3–[5–phenylpentan–2–yl] oxy–5, 6, 6a, 7, 8, 9, 10, 10a–octahydrophenanthridin–1–yl] acetate.
9-(Hydroxymethyl)–6, 6–dimethyl–3–(2–methyloctan–2–yl)–6a, 7, 10, 10a–tetrahydrobenzo[c]chromen–1–ol.
Nabilone.
Any compound structurally derived from 3–(1–naphthoyl)indole or 1H–indol–3–yl–(1–naphthyl)methane by substitution at the nitrogen atom of the indole ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2–(4–morpholinyl)ethyl, whether or not further substituted in the indole ring to any extent and whether or not substituted in the naphthyl ring to any extent.
Any compound structurally derived from 3–(1–naphthoyl)pyrrole by substitution at the nitrogen atom of the pyrrole ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2–(4–morpholinyl)ethyl, whether or not further substituted in the pyrrole ring to any extent and whether or not substituted in the naphthyl ring to any extent.
Any compound structurally derived from 1–(1–naphthylmethyl)indene by substitution at the 3–position of the indene ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2–(4–morpholinyl)ethyl, whether or not further substituted in the indene ring to any extent and whether or not substituted in the naphthyl ring to any extent.
Any compound structurally derived from 3–phenylacetylindole by substitution at the nitrogen atom of the indole ring with alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2–(4–morpholinyl)ethyl, whether or not further substituted in the indole ring to any extent and whether or not substituted in the phenyl ring to any extent.
Any compound structurally derived from 2–(3–hydroxycyclohexyl)phenol by substitution at the 5–position of the phenolic ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2–(4–morpholinyl)ethyl, whether or not further substituted in the cyclohexyl ring to any extent.]
Textual Amendments
F1Sch. 2 Pt. 2 para. 1(b) added by S.I. 1984/859, art. 2(3)
F2Words in Sch. 2 Pt. 2 para. 1(a) inserted (26.1.2009) by The Misuse of Drugs Act 1971 (Amendment) Order 2008 (S.I. 2008/3130), art. 2(2)(a)
F3Words in Sch. 2 Pt. 2 para. 1(a) deleted (29.1.2004) by The Misuse of Drugs Act 1971 (Modification) (No. 2) Order 2003 (S.I. 2003/3201), art. 2(3)
F4Word repealed by S.I. 1985/1995, art. 2(2)(a)
F5Word inserted by S.I. 1985/1995, art. 2(2)(b)
F6Word inserted by S.I. 1984/859, art. 2(3)
F7Words in Sch. 2 Pt. 2 para. 1(a) inserted (1.5.1998) by S.I. 1998/750, art. 2(3)
F8Word in Sch. 2 Pt. 2 para. 1(a) repealed (18.1.2007) by The Misuse of Drugs Act 1971 (Amendment) Order 2006 (S.I.2006/3331), art. 2(2)
F9Word in Sch. 2 Pt. 2 para. 1(a) inserted (1.2.2002) by S.I. 2001/3932, art. 2(3)
F10Words inserted by S.I. 1973/771, art. 2
F11Word inserted by S.I. 1985/1995, art. 2(2)(c)
F12Word inserted by S.I. 1973/771, art. 2
F13Sch. 2 Pt. 2 para. 1(c) inserted (23.12.2009) by The Misuse of Drugs Act 1971 (Amendment) Order 2009 (S.I. 2009/3209), art. 2(2)(a)
2U.K.Any stereoisomeric form of a substance for the time being specified in paragraph 1 of this Part of this Schedule.
[F142A.U.K.Any ester or ether of cannabinol or of a cannabinol derivative [F15or of a substance for the time being specified in paragraph 1(c) of this Part of this Schedule.] .]
Textual Amendments
F14Sch. 2 Pt. 2 para. 2A inserted (26.1.2009) by Misuse of Drugs Act 1971 (Amendment) Order 2008 (S.I. 2008/3130), arts. 1(1), 2(2)(b)
F15Words in Sch. 2 Pt. 2 para. 2A inserted (23.12.2009) by Misuse of Drugs Act 1971 (Amendment) Order 2009 (S.I. 2009/3209), arts. 1, 2(2)(b)
3U.K.Any salt of a substance for the time being specified in paragraph 1 [F16, 2 or 2A] of this Part of this Schedule.
Textual Amendments
F16Words in Sch. 2 Pt. 2 para. 3 substituted ( 26.1.2009 ) by The Misuse of Drugs Act 1971 (Amendment) Order 2008 (S.I. 2008/3130), art. 2(2)(c)
4U.K.Any preparation or other product containing a substance or product for the time being specified in any of paragraphs 1 to 3 of this Part of this Schedule, not being a preparation falling within paragraph 6 of Part I of this Schedule.
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