Bill Text: HI SB1333 | 2022 | Regular Session | Amended
Bill Title: Relating To The Uniform Controlled Substances Act.
Spectrum: Partisan Bill (Democrat 4-0)
Status: (Engrossed - Dead) 2021-12-10 - Carried over to 2022 Regular Session. [SB1333 Detail]
Download: Hawaii-2022-SB1333-Amended.html
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THE SENATE |
S.B. NO. |
1333 |
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THIRTY-FIRST LEGISLATURE, 2021 |
S.D. 2 |
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STATE OF HAWAII |
H.D. 2 |
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A BILL FOR AN ACT
RELATING TO THE UNIFORM CONTROLLED SUBSTANCES ACT.
BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF HAWAII:
SECTION 1. The legislature
finds that recent updates to the federal Controlled Substances Act require state
action in order to conform the State's Uniform Controlled Substances Act with federal
law.
The legislature recognizes that the Agriculture
Improvement Act of 2018, informally known as the 2018 "Farm Bill",
legalized hemp by removing hemp from the definition of "marihuana"
contained in the federal Controlled Substances Act.
The legislature further finds that, on August 28, 2020, the department of public safety received notice via publication in the Federal Register of an interim final order that the following substance was deleted from Schedule V of the federal schedule of controlled substances, title 21 Code of Federal Regulations section 1308.15, by the United States Drug Enforcement Administration: "[D]rug products in finished dosage formulations that have been approved by [the Federal Drug Administration] and that contain cannabidiol (CBD) derived from cannabis and no more than 0.1 per cent (w/w) residual tetrahydrocannabinols."
The legislature additionally finds that this federal scheduling action removes the regulatory controls and the administrative, civil, and criminal sanctions applicable to federal Schedule V controlled substances on persons who handle or propose to handle the drug products listed above.
For purposes of clarity, this Act specifically applies to the Federal Drug Administration-approved prescription drug Epidiolex and any generic versions of that drug that are Federal Drug Administration-approved and contain cannabidiol derived from cannabis and no more than 0.1 per cent (w/w) residual tetrahydrocannabinols only.
The legislature also finds that Epidiolex was approved by the Federal Drug Administration on June 25, 2018, for the treatment of seizures associated with Lennox-Gastaux syndrome and Dravet syndrome, two rare and difficult-to-treat forms of childhood-onset epilepsy, in patients two years of age or older. Epidiolex's effectiveness was studied in three randomized, double-blind, placebo-controlled clinical trials involving five hundred sixteen patients with either Lennox-Gastaux syndrome or Dravet. Epidiolex, taken along with other medications, was shown to be effective in reducing the frequency of seizures when compared with placebo. On July 31, 2020, the Federal Drug Administration approved Epidiolex for a new indication—the treatment of seizures associated with tuberous sclerosis complex, a rare genetic disease, in patients one year of age and older. Epidiolex is the only Federal Drug Administration‑approved drug that contains a purified drug substance derived from cannabis.
This Act should not be construed to change the legal status of cannabis, tetrahydrocannabinols, and other cannabis-related constituents, except as provided under federal law. Furthermore, unless further notice is given, the controls under federal and state law pertaining to prescription drugs continue to apply to Epidiolex and any generic versions of that drug that are Federal Drug Administration-approved and contain cannabidiol derived from cannabis and no more than 0.1 per cent residual tetrahydrocannabinols.
The purpose of this Act is to update the Uniform Controlled
Substances Act to be consistent with amendments in the federal controlled substances
law by:
(1) Exempting hemp from the Uniform Controlled Substances Act; and
(2) Removing cannabidiol drugs that have been approved by the United States Food and Drug Administration from the list of Schedule V substances and certain provisions of the Hawaii Penal Code.
SECTION 2. Section 329-1, Hawaii Revised Statutes, is amended by amending the definition of "marijuana" to read as follows:
""Marijuana" means all parts of the plant (genus) Cannabis whether growing or not; the seeds thereof, the resin extracted from any part of the plant; and every compound, manufacture, salt, derivative, mixture, or preparation of the plant, its seeds, or resin.
Marijuana shall not include:
(1) The mature stalks
of the plant (genus) Cannabis, fiber produced from the stalks, oil, or cake
made from the seeds of the plant, any other compound, manufacture, salt,
derivative, mixture, or preparation of the mature stalks (except the resin
extracted therefrom), fiber, oil, or cake, or the sterilized seed of the plant that
is incapable of germination; or
(2) Hemp [that is in
the possession, custody, or control of an individual or entity that holds a
license to produce hemp, issued by the Secretary of the United States Department
of Agriculture pursuant to title 7 United States Code section 1639q;
(3) Hemp that is in
the possession, custody, or control of a person or entity that is authorized
under state law to process hemp; and
(4) A product
containing or derived from hemp that:
(A) Does
not include any living hemp plants, viable seeds, leaf materials, or floral
materials; and
(B) Has
a delta-9-tetrahydrocannabinol concentration of not more than 0.3 per cent on a
dry weight basis, as measured post-decarboxylation or other similarly reliable
methods]."
SECTION 3. Section 329-14, Hawaii Revised Statutes, is amended by amending subsection (g) to read as follows:
"(g) Any of the following cannabinoids, their salts, isomers, and salts of isomers, unless specifically excepted, whenever the existence of these salts, isomers, and salts of isomers is possible within the specific chemical designation:
(1) Tetrahydrocannabinols;
meaning tetrahydrocannabinols naturally contained in a plant of the genus
Cannabis (cannabis plant), as well as synthetic equivalents of the substances
contained in the plant, or in the resinous extractives of Cannabis, sp. or
synthetic substances, derivatives, and their isomers with similar chemical
structure and pharmacological activity to those substances contained in the
plant, such as the following: Delta 1 cis or trans tetrahydrocannabinol, and
their optical isomers; Delta 6 cis or trans tetrahydrocannabinol, and
their optical isomers; and Delta 3,4 cis or trans-tetrahydrocannabinol, and its
optical isomers (since nomenclature of these substances is not internationally standardized,
compounds of these structures, regardless of numerical designation of atomic
positions, are covered); provided that tetrahydrocannabinols shall not
include any material, compound, mixture, or preparation that falls within the
definition of hemp;
(2) Naphthoylindoles; meaning any compound containing a 3-(1-naphthoyl)indole structure with substitution at the nitrogen atom of the indole ring by a alkyl, haloalkyl, alkenyl, cycloalkylmethyl,cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl or 2-(4-morpholinyl)ethyl group, whether or not further substituted in the indole ring to any extent and whether or not substituted in the naphthyl ring to any extent;
(3) Naphthylmethylindoles; meaning any compound containing a 1H-indol-3-yl-(1-naphthyl) methane structure with substitution at the nitrogen atom of the indole ring by a alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl) methyl or 2-(4-morpholinyl) ethyl group whether or not further substituted in the indole ring to any extent and whether or not substituted in the naphthyl ring to any extent;
(4) Naphthoylpyrroles; meaning any compound containing a 3-(1-naphthoyl)pyrrole structure with substitution at the nitrogen atom of the pyrrole ring by a alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl or 2-(4-morpholinyl) ethyl group whether or not further substituted in the pyrrole ring to any extent, whether or not substituted in the naphthyl ring to any extent;
(5) Naphthylmethylindenes; meaning any compound containing a naphthylideneindene structure with substitution at the 3-position of the indene ring by a alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl) methyl or 2-(4-morpholinyl) ethyl group whether or not further substituted in the indene ring to any extent, whether or not substituted in the naphthyl ring to any extent;
(6) Phenylacetylindoles; meaning any compound containing a 3-phenylacetylindole structure with substitution at the nitrogen atom of the indole ring by a alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl) methyl or 2-(4-morpholinyl) ethyl group whether or not further substituted in the indole ring to any extent, whether or not substituted in the phenyl ring to any extent;
(7) Cyclohexylphenols; meaning any compound containing a 2-(3-hydroxycyclohexyl) phenol structure with substitution at the 5-position of the phenolic ring by a alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl) methyl or 2-(4-morpholinyl) ethyl group whether or not substituted in the cyclohexyl ring to any extent;
(8) Benzoylindoles; meaning any compound containing a 3-(benzoyl) indole structure with substitution at the nitrogen atom of the indole ring by a alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl) methyl, or 2-(4-morpholinyl) ethyl group whether or not further substituted in the indole ring to any extent and whether or not substituted in the phenyl ring to any extent;
(9) [2,3-Dihydro-5-methyl-3-(4-morpholinylmethyl) pyrrolo[1,2,3-de]-1, 4-benzoxazin-6-yl]-1-naphthalenylmethanone (another trade name is WIN 55,212-2);
(10) (6a,10a)-9-(hydroxymethyl)-6, 6-dimethyl-3-(2-methyloctan-2-yl)-6a,7,10,10a-tetrahydrobenzo[c]chromen-1-ol (Other trade names are: HU-210/HU-211);
(11) Tetramethylcyclopropanoylindoles; meaning any compound containing a 3-tetramethylcyclopropanoylindole structure with substitution at the nitrogen atom of the indole ring by an alkyl, haloalkyl, cyanoalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, 2-(4-morpholinyl)ethyl, 1-(N-methyl-2-pyrrolidinyl)methyl, 1-(N-methyl-3-morpholinyl)methyl, or tetrahydropyranylmethyl group, whether or not further substituted in the indole ring to any extent and whether or not substituted in the tetramethylcyclopropyl ring to any extent;
(12) N-(1-adamantyl)-1-pentyl-1H-indazole-3-carboxamide, its optical, positional, and geometric isomers, salts, and salts of isomers (Other names: APINACA, AKB48);
(13) Quinolin-8-yl 1-pentyl-1H-indole-3-carboxylate, its optical, positional,
and geometric isomers, salts, and salts of isomers (Other names: PB-22; QUPIC);
(14) Quinolin-8-yl 1-(5fluoropentyl)-1H-indole-3-carboxylate, its optical,
positional, and geometric isomers, salts, and salts of isomers (Other names:
5-fluoro-PB-22; 5F-PB-22);
(15) N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide,
its optical, positional, and geometric isomers, salts, and salts of isomers
(Other names: AB-FUBINACA);
(16) N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-pentyl-1H-indazole-3-carboxamide,
its optical, positional, and geometric isomers, salts, and salts of isomers
(Other names: ADB-PINACA);
(17) N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(cyclohexylmethyl)-1H-indazole-3-carboxamide, its optical, positional, and geometric isomers, salts, and salts of isomers (Other names: AB-CHMINACA);
(18) N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-pentyl-1H-indazole-3-carboxamide,
and geometric isomers, salts, and salts of isomers (Other names: AB-PINACA);
(19) [1-(5-fluoropentyl)-1H-indazol-3-yl](naphthalen-1-yl)methanone,
and geometric isomers, salts, and salts of isomers (Other names: THJ-2201);
(20) Methyl (1-(4-fluorobenzyl)-1 H-indazole-3-carbonyl)-L-valinate, and geometric isomers, salts, and salts of isomers (Other names: FUB-AMB);
(21) (S)-methyl 2-(1-(5-fluoropentyl)-1H-indazole-3-carboxamido)-3-methylbutanoate, and geometric isomers, salts, and salts of isomers (Other names: 5-fluoro-AMB, 5-fluoro-AMP);
(22) N-((3s,5s,7s)-adamantan-1-yl)-1-(5-fluoropentyl)-1H-indazole-3-carboxamide, and geometric isomers, salts, and salts of isomers (Other names: AKB48 N-(5-fluoropentyl) analog, 5F-AKB48, APINACA 5-fluoropentyl analog, 5F-APINACA);
(23) N-adamantyl-1-fluoropentylindole-3-Carboxamide,
and geometric isomers, salts, and salts
of isomers (Other names: STS-135, 5F-APICA; 5-fluoro-APICA);
(24) Naphthalen-1-yl 1-(5-fluoropentyl)-1H-indole-3-carboxylate, and geometric isomers, salts, and salts of isomers (Other names: NM2201);
(25) N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-(cyclohexylmethyl)-1H-indazole-3-carboxamide, and geometric isomers, salts, and salts of isomers (Other names: MAB-CHMINACA and ADB-CHMINACA);
(26) Methyl 2-[1-(5-fluoropentyl)-1H-indazole-3-carboxamido]-3,3-dimethylbutanoate (Other names: 5F-ADB, 5-flouro-ADB, and 5F-MDMB-PINACA), its optical, positional, and geometric isomers, salts, and salts of isomers; and
SECTION 4. Section 329-22, Hawaii Revised Statutes, is amended to read as follows:
"§329-22 Schedule V. (a) The controlled substances listed in this section are included in schedule V.
(b)
Narcotic drugs containing nonnarcotic active medicinal ingredients. Any compound, mixture, or preparation
containing limited quantities of any of the following narcotic drugs, which
also contains one or more nonnarcotic active medicinal ingredients in
sufficient proportion to confer upon the compound, mixture, or preparation,
valuable medicinal qualities other than those possessed by the narcotic drug
alone:
(1) Not more than 200 milligrams of codeine, or any of its salts, per 100 milliliters or per 100 grams;
(2) Not more than 100 milligrams of dihydrocodeine,
or any of its salts, per 100 milliliters or per 100 grams;
(3) Not more than 100 milligrams of ethylmorphine, or
any of its salts, per 100 milliliters or per 100 grams;
(4) Not more than 2.5 milligrams of diphenoxylate and
not less than 25 micrograms of atropine sulfate per dosage unit;
(5) Not more than 100 milligrams of opium per 100 milliliters
or per 100 grams; and
(6) Not more than 0.5 milligram of difenoxin and not
less than 25 micrograms of atropine sulfate per dosage unit.
(c) Stimulants. Unless specifically exempted or excluded or
unless listed in another schedule, any material, compound, mixture, or
preparation that contains any quantity of the following substances having a stimulant
effect on the central nervous system, including its salts, isomers, and salts
of isomers.
(d) Depressants.
Unless specifically exempted or excluded or unless listed in another
schedule, any material, compound, mixture, or preparation that contains any
quantity of the following substances having a depressant effect on the central
nervous system, including its salts, isomers, and salts of isomers:
(1) Lacosamide [(R)-2-acetoamido-N-benzyl-3-methoxy-propionamide], (Vimpat);
(2) Pregabalin [(S)-3-(aminomethyl)-5-methylhexanoic acid]; and
(3) Brivaracetam ((2S)-2-[(4R)-2-oxo-4-propylpyrrolidin-1-yl]butanamide) (Other names: BRV; UCB-34714; Briviact) and its salts.
[(e) Approved cannabidiol drugs. A drug product in finished dosage formulation
that has been approved by the United States Food and Drug Administration that
contains cannabidiol (2-[1R-3-methyl-6R-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol)
derived from cannabis and no more than 0.1 per cent (w/w) residual tetrahydrocannabinols.]"
SECTION 5. Section 712-1240, Hawaii Revised Statutes, is amended by amending the definitions of "marijuana" and "marijuana concentrate" to read as follows:
""Marijuana" means any part of the plant (genus) cannabis, whether growing or not, including the seeds and the resin, and every alkaloid, salt, derivative, preparation, compound, or mixture of the plant, its seeds or resin, except that, as used herein, "marijuana" shall not include:
(1) Hashish, tetrahydrocannabinol, and any alkaloid, salt, derivative, preparation, compound, or mixture, whether natural or synthesized, of tetrahydrocannabinol;
(2) Hemp that is in the
possession, custody, or control of an individual or entity that holds a license
to produce hemp issued by the United States Department of Agriculture pursuant
to title 7 [[]United States[]] Code section 1639q;
(3) Hemp that is in
the possession, custody, or control of a person or entity that is authorized
under state law to process hemp; [or]
(4) A product containing or derived from hemp that:
(A) Does not include any living hemp plants, viable seeds, leaf materials, or floral materials; and
(B) Has a delta-9-tetrahydrocannabinol
concentration of not more than 0.3 per cent, as measured post-decarboxylation
or other similarly reliable methods[.]; or
(5) A drug product in finished dosage formulation that has been approved by the United States Food and Drug Administration that contains cannabidiol (2-[1R-3-methyl-6R-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol) derived from cannabis and no more than 0.1 per cent (w/w) residual tetrahydrocannabinols.
"Marijuana concentrate" means hashish, tetrahydrocannabinol, or any alkaloid, salt, derivative, preparation, compound, or mixture, whether natural or synthesized, of tetrahydrocannabinol, except that, as used herein, "marijuana concentrate" shall not include:
(1) Hemp that is in
the possession, custody, or control of an individual or entity that holds a license
to produce hemp, issued by the Secretary of the United States Department of
Agriculture pursuant to title 7 United States Code section 1639q; [or]
(2) A product containing or derived from hemp, including any product containing one or more hemp-derived cannabinoids such as cannabidiol, that:
(A) Does not include any living hemp plants, viable seeds, leaf materials, or floral materials; and
(B) Has a delta-9-tetrahydrocannabinol
concentration of not more than 0.3 per cent, as measured post-decarboxylation
or other similarly reliable methods[.]; or
(3) A drug product in finished dosage formulation that has been approved by the United States Food and Drug Administration that contains cannabidiol (2-[1R-3-methyl-6R-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol) derived from cannabis and no more than 0.1 per cent (w/w) residual tetrahydrocannabinols."
SECTION 6. Act 14, Session Laws of Hawaii 2020, is amended by amending section 9 to read as follows:
"SECTION
9. This Act shall take effect upon its approval,
and shall be repealed on June 30, 2022[;], except that section 4 of this
Act shall not be repealed; provided that the [definition of
"marijuana" in section 329-1, Hawaii Revised Statutes, and the]
definitions of "marijuana" and "marijuana [Concentrate"]
concentrate" in section 712-1240, Hawaii Revised Statutes, shall be
reenacted in the form in which they read on the day prior to the effective date
of this Act."
SECTION 7. Statutory material to be repealed is bracketed and stricken. New statutory material is underscored.
SECTION 8. This Act shall take effect on January 1, 2050; provided that the amendments made to section 712-1240, Hawaii Revised Statutes, by section 5 of this Act shall not be repealed when that section is repealed and reenacted pursuant to section 9 of Act 14, Session Laws of Hawaii 2020.
Report Title:
Uniform Controlled Substances Act; Hawaii Penal Code; Hemp
Description:
Updates the Uniform Controlled Substances Act to be consistent with amendments in the federal controlled substances law. Exempts hemp from the Uniform Controlled Substances Act. Removes cannabidiol drugs that have been approved by the United States Food and Drug Administration from the list of Schedule V substances and certain provisions of the Hawaii Penal Code. Effective 1/1/2050. (HD2)
The summary description
of legislation appearing on this page is for informational purposes only and is
not legislation or evidence of legislative intent.
