APPENDIX B
Title 63
Crimes and Punishment
(Trust Territory
Code (1980))
CHAPTER 4
CONTROLLED SUBSTANCES
General Provisions
§251. Short title. This chapter may be cited as the "Trust Territory Controlled Substances Act." (P.L. No. 5-110.)
Source: 63 TTC 4 § 252,
modified.
§252. Definitions.
As used in this chapter:
(1)
"Administer" means the direct application of a controlled substance,
whether by injection, inhalation, ingestion, or any other means to the
body of a patient or research subject by:
(a) A practitioner (or, in his presence, by his
authorized agent), or
(b) The patient or research subject at the
direction and in the presence of the practitioner.
(2)
"Agent" means an authorized person who acts on behalf of or at the
direction of a manufacturer, distributor, or dispenser but does not
include a common or contract carrier, public warehouseman, or employee
thereof.
(3)
"Controlled substance" means a drug, substance, or immediate
precursor in schedules I through V of subchapter II of this
chapter.
(4)
"Counterfeit substance" means a controlled substance which, or the
container or labeling of which, without authorization, bears the
trademark, trade name, or other identifying mark, imprint, number or
device, or any likeness thereof, of a manufacturer, distributor, or
dispenser other than the person or persons who in fact manufactured,
distributed, or dispensed such substance and which thereby falsely
purports or is represented to be the product of, or to have been
distributed by, such other manufacturer, distributor, or
dispenser.
(5)
"Deliver" or "Delivery" means the actual, constructive, or attempted
transfer of a controlled substance whether or not there exists an agency
relationship.
(6)
"Director" means the director of the department of health services
of the government of the Trust Territory.
(7)
"Dispense" means to deliver a controlled substance to the ultimate
user or human research subject by or pursuant to the lawful order of a
practitioner, including prescribing, administering, packaging, labeling,
and compounding necessary to prepare the substance for such
delivery.
(8)
"Dispenser" is a practitioner who dispenses.
(9)
"Distribute" means to deliver other than by administering or
dispensing a controlled substance.
(10)
"Distributor" means a person who distributes.
(11)
"Drug" means (a) substances recognized in the official United States
pharmacopoeia, official homeopathic pharmacopoeia of the United States, or
official national formulary, or any supplement to any of them, and (b)
substances intended for use in the diagnosis, cure, mitigation, treatment,
or prevention of disease in man or other animals, and (c) substances
(other than food) intended to affect the structure or any function of the
body of man or other animals, and (d) substances intended for use as a
component of any article specified in clause (a), (b), or (c) of this
paragraph, but does not include devices or their components, parts, or
accessories.
(12)
"Drug dependent person" means a person who is using a controlled substance
and who is in a state of psychic or physical dependence, or both, arising
from administration of that controlled substance on a continuous basis.
Drug dependence is characterized by behavioral and other responses which
include a strong compulsion to take the substance on a continuous basis in
order to experience its psychic effects, or to avoid the discomfort of its
absence.
(13)
"Manufacture" means the production, preparation, propagation,
compounding, conversion or processing of a controlled substance, either
directly or indirectly by extraction from substances of natural origin, or
independently by means of chemical synthesis, or by a combination of
extraction and chemical synthesis, and includes any packaging or
repackaging of the substance or labeling or relabeling of its container,
except that this term does not include the preparation or compounding of a
controlled substance by an individual for his own use or the preparation,
compounding, packaging, or labeling of a controlled
substance:
(a) By a practitioner
as an incident to his administering or dispensing of a controlled
substance in the course of his professional practice, or
(b) By a practitioner,
or by his authorized agent under his supervision, for the purpose of, or
as an incident to research, teaching, or chemical analysis and not for
sale.
(14)
"Marihuana" means all parts of the plant cannabis sativa L., whether
growing or not, the seeds thereof, the resin extracted from any part of
such plant, and every compound, manufacture, salt, derivative, mixture, or
preparation of such plant, its seeds or resin, but shall not include the
mature stalks of such plant, fiber produced from such stalks, oil or cake
made from the seeds of such plant, any other compound, manufacture, salt,
derivative, mixture, or preparation of such mature stalks (except the
resin extracted therefrom), fiber, oil, or cake, or the sterilized seed of
such plant which is incapable of germination.
(15)
"Narcotic drug" means any of the following whether produced directly
or indirectly by extraction from substances of vegetable origin, or
independently by means of chemical synthesis, or by a combination of
extraction and chemical synthesis:
(a) Opium and opiate,
and any salt, compound, derivative, or preparation of opium or
opiate.
(b) Any salt,
compound, isomer, derivative, or preparation thereof which is chemically
equivalent or identical with any of the substances referred to in clause
(a), above, but not including the isoquinoline alkaloids of
opium.
(c) Opium poppy and
poppy straw.
(d) Coca leaves and
any salt, compound, derivative, or preparation of coca leaves, and any
salt, compound, isomer, derivative, or preparation thereof which is
chemically equivalent or identical with any of these substances, but not
including decocainized coca leaves or extractions of coca leaves which do
not contain cocaine or ecgonine.
(16)
"Opiate" means any substance having an addiction-forming or
addiction-sustaining liability similar to morphine or being capable of
conversion into a drug having addiction-forming or addiction-sustaining
liability. It does not include, unless specifically designated as
controlled under section 256 of this title, the dextrorotatory isomer of
3-methoxy-n-methylmorphinan and its salts (dextromethorphan). It does
include its racemic and levorotatory forms.
(17)
"Opium poppy" means the plant of the species papaver somniferum L.,
except the seeds thereof.
(18)
"Person" means any individual, corporation, government or
governmental subdivision or agency, business trust, estate, trust,
partnership or association, or any other legal entity.
(19)
"Poppy straw" means all parts, except the seeds of the opium poppy,
after mowing.
(20)
"Practitioner" means:
(a) A physician,
dentist, veterinarian, scientific investigator, or other person licensed,
registered or otherwise authorized by the director to distribute,
dispense, conduct research with respect to or to administer a controlled
substance in the course of professional practice or research in this
territory.
(b) A pharmacy,
hospital or other institution licensed, registered or otherwise authorized
by the director to distribute, dispense, conduct research with respect to
or to administer a controlled substance in the course of professional
practice or research in the Trust Territory.
(21)
"Production" includes the manufacture, planting, cultivation,
growing, or harvesting of a controlled substance.
(22)
"Immediate precursor" means a substance which the director has found
to be and by regulation designates as being the principal compound
commonly used or produced primarily for use, and which is an immediate
chemical intermediary used or likely to be used in the manufacture of a
controlled substance, the control of which is necessary to prevent,
curtail, or limit such manufacture.
(23)
"Ultimate user" means a person who lawfully possesses a controlled
substance for his own use or for the use of a member of his household or
for administration to an animal owned by him or by a member of his
household.
(24)
"Federal law" means a law enacted by the Congress of the United
States. (P.L. No. 5-110.)
Source: 63 TTC 4 § 252,
modified.
Standards and
Schedules
§256. Reports and recommendations by director to congress;
amendment of schedule by congress.
(1)
Annually, upon the convening of each annual session of the Congress
of Micronesia, the director shall report to the Congress of Micronesia the
effects of the implementation of this chapter in relation to the problems
of drug abuse in the Trust Territory, and shall recommend to the Congress
of Micronesia any additions, deletions or revisions in the schedules of
substances enumerated in sections 259, 261, 263, 265 and 267 of this
title, and any other recommendations which he deems necessary. The
director shall not recommend any additions, deletions or revisions in such
schedules until after notice and an opportunity for a hearing is afforded
all interested parties, except such hearing shall not be required if
official notice has been received that the substance has been added,
deleted or rescheduled as a controlled substance under federal law. In
making a determination regarding a substance, the director shall assess
the degree of danger or probable danger of the substance by considering
the following:
(a) The actual or
probable abuse of the substance including:
(i) Its history and current pattern of
abuse;
(ii) The scope, duration and significance of
abuse; and
(iii) A judgment of the degree of actual or
probable detriment which may result from the abuse of the
substance.
(b) The biomedical hazard of the substance
including:
(i) Its pharmacology: the effects and modifiers
of effects of the substance;
(ii) Its toxicology: the acute and chronic
toxicity, interaction with other substances whether controlled or not and
liability to psychic or physiological dependence;
(iii) Risk to public health and particular
susceptibility of segments of the population; and
(iv) Existence of therapeutic alternatives for
substances which are or may be used for medical purposes.
(c) A judgment of the probable physical and
social impact of widespread abuse of the substance.
(d) Whether the substance is an immediate
precursor of a substance already controlled under this
part.
(e) The current state of scientific knowledge
regarding the substance.
(2)
After considering the factors enumerated above, the director shall
make a recommendation to the Congress of Micronesia, specifying to what
schedule the substance shall be added, deleted or rescheduled if it finds
that the substance has a degree of danger or probable danger. The
director may make such recommendation to the Congress of Micronesia prior
to the submission of its annual report in which case the director shall
publish and give notice to the public of such
recommendation.
(3)
The Congress of Micronesia has the sole authority to add, delete, or
reschedule all substances enumerated in the schedules in sections 259,
261, 263, 265 and 267 of this title.
(4)
If the Congress of Micronesia designates a substance as an immediate
precursor, substances which are precursors of the controlled precursor
shall not be subject to control solely because they are precursors of the
controlled precursor.
(5) If a substance is added,
deleted or rescheduled as a controlled substance under federal law and
notice of the designation is given to the director, the director shall
recommend that a corresponding change in Trust Territory law be made by
the Congress of Micronesia, unless the director objects to the
change. In that case, the director shall publish the reasons
for objection and afford all interested parties an opportunity to be
heard. Following the hearing, the director shall announce his decision and
shall notify the Congress of Micronesia in writing of the change in
federal law or regulations and of the director's recommendations. (P.L.
No. 5-110.)
Source: 63 TTC 4 § 256,
modified.
§257. Nomenclature.
The following schedules include the controlled substances listed or
to be listed by whatever official name, common or usual name, chemical
name or trade name designated. (P.L. No. 5-110.)
Source: 63 TTC 4 § 257,
modified.
§258. Schedule I; criteria for classification.
The director in his recommendation shall place a substance in
schedule I if he finds that the substance:
(1)
Has a high potential for abuse; and
(2)
Has no accepted medical use in treatment in the United States, or
lacks accepted safety for use in treatment under medical supervision.
(P.L. No.5-110.)
Source: 63 TTC 4 § 258,
modified.
§259. Same; schedule I.
The controlled substances listed in this section are included in
schedule I:
(1)
Any of the following opiates, including their isomers, esters,
ethers, salts, and salts of isomers, esters, and ethers, unless
specifically excepted, whenever the existence of such isomers, esters,
ethers and salts is possible within the specific chemical
designation:
1.
Acetylmethadol.
2.
Allylprodine.
3.
Alphacetylmethadol.
4.
Alphameprodine.
5.
Alphamethadol.
6.
Bensethidine.
7.
Betacetylmethadol.
8.
Betameprodine.
9.
Betamethadol.
10.
Betaprodine.
11.
Clonitazene.
12.
Dextromoramide.
13.
Dextrorphan.
14.
Diampromide.
15.
Diethyliambutene.
16.
Dimenoxadol.
17.
Dimepheptanol.
18.
Dimethylthiambutene.
19.
Dioxaphetylbutyrate.
20.
Dipipanone.
21.
Ethylmethylthiambutene.
22.
Etonitazene.
23.
Etoxeridine.
24.
Furethidine.
25.
Hydroxpethidine.
26.
Ketobemidone.
27.
Lavomoramide.
28.
Levophenacylmorphan.
29.
Morpheridine.
30.
Noracymethadol.
31.
Norlevorphanol.
32.
Normethadone.
33.
Norpipanone.
34.
Phenadoxone.
35.
Phenampromide.
36.
Phenomorphan.
37.
Phenoperidine.
38.
Piritramide.
39.
Proheptazine.
40.
Properidine.
41.
Propiram.
42.
Racemoramide.
43.
Trimeperidine.
(2)
Any of the following opium derivatives, their salts, isomers and
salts of isomers, unless specifically excepted, whenever the existence of
such salts, isomers and salts of isomers is possible within the specific
chemical designation:
1.
Acetorphine.
2.
Acetyldihydrocodeine.
3.
Benzylmorphine.
4.
Codeine methylbromide.
5.
Codeine-N-Oxide.
6.
Cyprenorphine.
7.
Desoporphine.
8.
Dihydromorphine.
9.
Drotebanol.
10.Etorphine (Except hydrochloride salt).
11.
Heroin.
12.
Hydromorphinol.
13.
Methyldesorphine.
14.
Methyldihydromorphine.
15.
Morphine methylbromide.
16.
Morphine methylsulfonate.
17.
Morphine-N-Oxide.
18.
Myrophine.
19.
Nicocodeine.
20.
Nicomorphine.
21.
Normorphine.
22.
Phoclodine.
23.
Thebacon.
(3)
Any material, compound, mixture or preparation which contains any
quantity of the following hallucinogenic substances, their salts, isomers
and salts of isomers, unless specifically excepted, whenever the existence
of such salts, isomers, and salts of isomers is possible within the
specific chemical designation:
1. 2,5
dimethoxyamphetamine (2,5-DMA).
2.
3,4-methylenedioxyamphetamine.
3.
5-methoxy-3,4-methylenedioxyamphetamine.
4.
4-bromo-2,5 dimethoxyamphetamine (4-bromo-2,5-DMA).
5.
3,4,5-trimethoxyamphetamine.
6.
Bufotenine.
7.
4-methoxyamphetamine (PMA).
8.
Diethyltryptamine.
9.
Dimethyltryptamine.
10.
4-methyl-2,5-dimethoxylamphetamine.
11.
Ibogaine.
12.
Lysergic acid diethylamide.
13.
Marihuana.
14.
Mescaline.
15.
Peyote.
16.
N-ethyl-3-piperidyl benzilate.
17.
N-methyl-3-piperidyl benzilate.
18.
Psilocyn.
19.
Psilocybin.
20.
Tetrahydrocannabinol. (P.L. No. 5-110.)
§260. Schedule II; criteria for classification. The director in his recommendation shall
place a substance in schedule II if he finds that:
(1)
the substance has a high potential for abuse;
(2)
the substance has currently accepted medical use with severe
restrictions; and
(3)
abuse of the substance may lead to severe psychic or physical
dependence. (P.L. No. 5-110.)
Source: 63 TTC 4 § 260,
modified.
§261. Same; schedule II.
The controlled substances listed in this section are included in
schedule II:
(1)
Any of the following substances except those narcotic drugs listed
in other schedules, whether produced directly or indirectly by extraction
from substances of vegetable origin, or independently by means of chemical
synthesis, or by combination of extraction and chemical
synthesis:
(a) Opium and opiate,
and any salt, compound, derivative, or preparation of opium or
opiate;
(b) Any salt,
compound, isomers, derivative or preparation thereof which is chemically
equivalent or identical with any of the substances referred to in (a),
above, but not including the isoquinoline alkaloids of
opium;
(c) Opium poppy and
poppy straw;
(d) Coca leaves and
any salt, compound, derivative, or preparation of coca leaves, and any
salt, compound, derivative or preparation thereof which is chemically
equivalent or identical with any of these substances, but not including
decocainized coca leaves or extractions which do not include cocaine or
ecgonine.
(2)
Any of the following opiates, including their immediate isomers,
esters, ethers, salts, and salts of isomers, ester and ethers, unless
specifically excepted, whenever the existence of such isomers, esters,
ethers and salts is possible within the specific chemical
designation:
1.
Alphaprodine.
2.
Anileridine.
3.
Apomorphine.
4.
Bezitramide.
5.
Dihydrocodeine.
6.
Diphenoxylate.
7.
Fentanyl.
8.
Isomethadone.
9.
Levomethorphan.
10.
Levorphanol.
11.
Metazocine.
12.
Methadone.
13.
Methadone Intermediate, 4-cyano-2-dimethylamino-4, 4-diphenyl
butane.
14.
Methaqualone.
15.
Moramide Intermediate, 2-methyl-3-morpholino-1,
1-diphenyl-propane-carboxylic acid.
16.
Pethidine.
17.
Pethidine Intermediate A,
4-cyano-1-methyl-4-phenylpiperidine.
18.
Pethidine Intermediate B, ethyl-4-phenylpiperidine;
4-carboxylate.
19.
Pethidine Intermediate C, 1-methyl-4-phenylpiperidine-4-carboxylic
acid.
20.
Phenazocine.
21.
Piminodine.
22.
Racemethorphan.
23.
Racemorphan.
(3)
Any material, compound, mixture, or preparation which contains any
quantity of the following substances having a potential for abuse
associated with a stimulant effect on the central nervous
system:
(a) Amphetamine, its salts, optical isomers,
and salts of its optical isomers;
(b) Any substance which contains any quantity
of methamphetamine, including its salts, isomers, and salts of
isomers;
(c) Any material, compound, mixture, or
preparation which contains any quantity of the following substances having
a potential for abuse associated with a stimulant effect on the central
nervous system:
(1)
Phenmetrazine and its salts.
(2)
Methylphenidate. (P.L. No. 5-110.)
Source: 63 TTC 4 §
261, modified.
§262. Schedule III; criteria for classification. The director in his recommendation shall
place a substance in schedule III if he finds that:
(1)
The substance has a potential for abuse less than the substances
listed in schedules I and II;
(2)
The substance has currently accepted medical use in treatment in the
United States; and
(3)
Abuse of the substance may lead to moderate or low physical
dependence or high psychological dependence. (P.L. No.
5-110.)
Source: 63 TTC 4 § 262,
modified.
§263. Same; schedule III. The controlled substances listed in this
section are included in schedule III:
(1)
Unless listed in another schedule any material, compound, mixture,
or preparation which contains any quantity of the following substances
having a potential for abuse associated with a depressant effect on the
central nervous system:
(a) Any substance which contains any quantity
of a derivative of barbituric acid, or any salt of a derivative of
barbituric acid, except those substances which are specifically listed in
other schedules.
(b)
Benzphetamine.
(c) Chlorhexadol.
(d) Chlorphentermine.
(e) Chlortermine.
(f) Clutethimide.
(g) Diethylpropion.
(h) Lysergic acid.
(i) Lysergic acid amide.
(j) Mazindol.
(k) Methyproylon.
(l) Phencyclidine.
(m) Phendimetrazine.
(n) Phentermine.
(o) Sulfondiethylmethane.
(p) Sulfonethylmethane.
(q) Sulfonmethane.
(2)
Nalorphine.
(3)
Any material, compound, mixture, or preparation containing limited
quantities of any of the following narcotic drugs, or any salts
thereof:
(a) Not more than 1.8 grams of codeine, or any
of its salts, per 100 milliliters or not more than 90 milligrams per
dosage unit, with an equal or greater quantity of an isoquinoline alkaloid
of opium;
(b) Not more than 1.8 grams of codeine, or any
of its salts, per 100 milliliters or not more than 90 milligrams per
dosage unit, with one or more active, non-narcotic ingredients in
recognized therapeutic amounts;
(c) Not more than 300 milligrams of
dihydrocodeinone, or any of its salts, per 100 milliliters or not more
than 15 milligrams per dosage unit, with a fourfold or greater quantity of
an isoquinoline alkaloid of opium;
(d) Not more than 300 milligrams of
dihydrocodeinone, or any of its salts, per 100 milliliters or not more
than 15 milligrams per dosage unit, with one or more active, non-narcotic
ingredients in recognized therapeutic amounts;
(e) Not more than 1.8 grams of dihydrocodeine,
or any of its salts, per 100 milliliters or not more than 90 milligrams
per dosage unit, with one or more active, non-narcotic ingredients in
recognized therapeutic amounts;
(f) Not more than 300 milligrams of
ethylmorphine, or any of its salts, per 100 milliliters or not more than
15 milligrams per dosage unit, with one or more active, non-narcotic
ingredients in recognized therapeutic amounts;
(g) Not more than 500 milligrams of opium per
100 milliliters or per 100 grams, or not more than 25 milligrams per
dosage unit, with one or more active non-narcotic ingredients in
recognized therapeutic amounts;
(h) Not more than 50 milligrams of morphine, or
any of its salts, per 100 milliliters or per 100 grams with one or more
active, non-narcotic ingredients in recognized therapeutic
amounts.
(4)
The director may except by rule any compound, mixture, or
preparation containing any stimulant or depressant substance listed in
paragraphs (2) and (3) of this schedule above from the application of all
or any part of this chapter if the compound, mixture, or preparation
contains one or more active medicinal ingredients not having a stimulant
or depressant effect on the central nervous system, and if the admixtures
are included therein in combinations, quantity, proportion, or
concentration that vitiate the potential for abuse of the substances which
do have a stimulant or depressant effect on the central nervous system.
(P.L. No. 5-110.)
Source: 63 TTC 4 § 263,
modified.
§264. Schedule IV; criteria for classification.
The director in his recommendation shall place a substance in
schedule IV if he finds that:
(1)
The substance has a low potential for abuse relative to substances
in schedule III;
(2)
The substance has currently accepted medical use in treatment in the
United States; and
(3)
Abuse of the substance may lead to limited physical dependence or
psychological dependence relative to the substances listed in schedule
III. (P.L. NO. 5-110.)
Source: 63 TTC 4 § 264,
modified.
§265. Same; schedule IV. The controlled substances listed in this
section are included in schedule IV:
(1)
Any material, compound, mixture, or preparation which contains any
quantity of the following substances or salts thereof having a potential
for abuse associated with a depressant effect on the central nervous
system:
1.
Barbital.
2.
Chloral betaine.
3.
Chloral hydrate.
4.
Diethylpropion.
5.
Ethchlorvynol.
6.
Ethinamate.
7.
Fenfluramine.
8.
Methohexital.
9.
Meprobamate.
10.
Methylphenobarbital.
11.
Paraldehyde.
12.
Petrichloral.
13.
Phenobarbital.
(2)
The director may except by rule any compound, mixture, or
preparation containing any depressant substance listed in paragraph (1)
from the application of all or any part of this chapter if the compound,
mixture, or preparation contains one or more active medicinal ingredients
not having adepressant effect on the central nervous system, and if the
admixtures are included therein in combinations, quantity, proportion, or
concentration that vitiate the potential for abuse of the substances which
have a depressant effect on the central nervous system. (P.L. No.
5-110.)
Source: 63 TTC 4 § 265,
modified.
§266. Schedule V; criteria for classification. The director in his recommendation shall
place a substance in schedule V if he finds that:
(1)
The substance has a low potential for abuse relative to the
controlled substances listed in schedule IV;
(2)
The substance has currently accepted medical use in treatment in the
United States; and
(3)
The substance has limited physical dependence or psychological
dependence liability relative to the controlled substances listed in
schedule IV. (P.L. No. 5-110.)
Source: 63 TTC 4 § 266,
modified.
§267. Same; schedule V. The controlled
substances listed in this section are included in schedule V:
(1)
Any compound, mixture, or preparation containing limited quantities
of any of the following narcotic drugs, which shall include one or more
non-narcotic 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:
(a) Not more than 200 milligrams of codeine, or
any of its salts, per 100 milliliters or per 100 grams.
(b) Not more than 100 milligrams of
dihydrocodeine, or any of its salts, per 100 milliliters or per 100
grams.
(c) Not more than 100 milligrams of
ethylmorphine, or any of its salts, per 100 milliliters or per 100
grams.
(d) Not more than 2.5 milligrams of
dephenoxylate, and not less than 25 micrograms of atropine sulfate per
dosage unit.
(e) Not more than 100 milligrams of opium per
100 milliliters or per 100 grams, or not more than 5 milligrams per dosage
unit. (P.L. No. 5-110.)
Source: 63 TTC 4 § 267,
modified.
§268. Annual revision and republication of
schedules. The director shall
revise and republish the schedules annually and make them available to any
registrant, law enforcement agency or any member of the public desiring
such list. (P.L. No. 5-110.)
Source: 63 TTC 4 § 268,
modified.
Manufacture, Distribution,
and Dispensing
§271.
Authority of
director to promulgate rules and regulations. The director is authorized to promulgate
rules in accordance with chapter 1 of title 17 of this Code and charge
reasonable fees relating to the registration and control of the
manufacture, distribution, and dispensing of controlled substances within
the Trust Territory. (P. L. No. 5-110.)
Source: 63 TTC 4 § 271,
modified.
§272. Registration; required; exceptions.
(1)
Every person who manufactures, distributes, or dispenses any
controlled substance within the Trust Territory or who proposes to engage
in the manufacture, distribution, or dispensing of any controlled
substance within the Trust Territory shall obtain annually a registration
issued by the director in accordance with the rules made by
him.
(2)
Persons registered by the director under this chapter to
manufacture, distribute, dispense, or conduct research with controlled
substances may possess, manufacture, distribute, dispense, or conduct
research with those substances to the extent authorized by their
registration and in conformity with the other provisions of this
subchapter.
(3)
The following persons need not register and may lawfully possess
controlled substances under the provision of this chapter:
(a) A common or contract carrier or
warehouseman, or an employee thereof, whose possession of any controlled
substance is in the usual course of his business or
employment.
(b) An ultimate user or a person in possession
of any controlled substance pursuant to a lawful order of a practitioner
or in lawful possession of a schedule V substance.
(4)
The director may, by rule, waive the requirement for registration of
certain manufacturers, distributors, or dispensers if he finds it
consistent with the public health and safety.
(5)
A separate registration shall be required at each principal place of
business or professional practice where the applicant manufactures,
distributes, or dispenses controlled substances.
(6)
The director or his designee may inspect the establishment of a
registrant or applicant for registration in accordance with the rules
promulgated by him. (P.L. No. 5-110.)
Source: 63 TTC 4 § 272,
modified.
§273. Same; criteria for granting; effect; compliance with
federal law.
(1)
The director shall register an applicant to manufacture or
distribute controlled substances included in schedules I through V of
subchapter II of this chapter unless he determines that the issuance of
that registration is inconsistent with the public interest. In determining
the public interest, the director shall consider the following
factors:
(a) Maintenance of effective controls against
diversion of controlled substances into other than legitimate medical,
scientific, or industrial channels;
(b) Compliance with applicable
law;
(c) Prior conviction record of applicant under
federal, state and local laws relating to controlled
substances;
(d) Past experience in the manufacture or
distribution of controlled substances, and the existence in the
establishment of effective controls against diversion;
(e) Furnishing by the applicant of false or
fraudulent material in any application filed under this
chapter;
(f) Suspension or revocation of the applicant's
federal registration to manufacture, distribute, or dispense controlled
substances as authorized by federal law; and
(g) Any other factors relevant to and
consistent with the public health and safety.
(2)
Registration granted under paragraph (1) of this section shall not
entitle a registrant to manufacture and distribute controlled substances
in schedule I or II other than those specified in the registration.
(3)
Practitioners must be registered to dispense any controlled
substances or to conduct research with controlled substances in schedules
II through V if they are authorized to dispense or conduct research under
the law of the Trust Territory. The director need not require
separate registration under this subchapter for practitioners engaging in
research with non-narcotic controlled substances in schedules II through V
where the registrant is already registered under this subchapter in
another capacity. Practitioners registered under federal law to
conduct research with schedule I substances may conduct research with
schedule I substances within the Trust Territory upon furnishing evidence
of that federal registration.
(4)
Compliance by manufacturers and distributors with the provisions of
the federal law respecting registration (excluding fees) shall be deemed
compliance with this section. (P.L. No. 5-110.)
Source: 63 TTC 4 § 273,
modified.
§274. Same; revocation or suspension; grounds; limitation
of effect; sealing of substances; notice to bureau.
(1)
A registration pursuant to section 273 of this title to manufacture,
distribute, or dispense a controlled substance, may be suspended or
revoked by the director upon a finding that the
registrant:
(a) Has materially falsified any application
filed pursuant to this chapter or required by this
chapter;
(b) Has been convicted of any violation under
this chapter or any law of the United States, or of any state or
territory, relating to any substance defined herein as a controlled
substance; or
(c) Has had his federal registration suspended
or revoked by competent federal authority and is no longer authorized by
federal law to engage in the manufacture, distribution, or dispensing of
controlled substances; or
(d) Has violated any regulation promulgated by
the director relating to subchapter III of this chapter;
(e) Will abuse or unlawfully transfer such
substances or that the registrant will fail to safeguard adequately his
supply of such substances against diversion into other than legitimate
channels of distribution.
(2)
The director may limit revocation or suspension of a registration to
the particular controlled substance with respect to which grounds for
revocation or suspension exists.
(3)
In the event the director suspends or revokes a registration granted
under section 273 of this title all controlled substances owned or
possessed by the registrant pursuant to such registration at the time of
suspension or the effective date of the revocation order, as the case may
be, may in the discretion of the director be placed under seal. No
disposition may be made of substances under seal until the time for taking
an appeal has elapsed or until all appeals have been concluded unless a
court, upon application therefor, orders the sale of perishable substances
and the deposit of the proceeds of the sale with the court. Upon a
revocation order becoming final, all such controlled substances shall be
forfeited.
(4)
The bureau shall promptly be notified of all orders suspending or
revoking registration and all forfeitures of controlled substances. (P.L.
No. 5-110.)
Source: 63 TTC 4 § 274,
modified.
§275. Same; same; notice and hearing.
(1)
Before denying, suspending or revoking a registration, or refusing a
renewal of registration, the director shall serve upon the applicant or
registrant in accordance with chapter 1 of title 17 of this Code notice to
show cause why registration should not be denied, revoked, or suspended,
or why the renewal should not be refused. The notice to show cause
shall contain a statement of the basis therefor and shall call upon the
applicant or registrant to appear before the director at a time and place
not less than thirty days after the date of service of the notice, but in
the case of a denial or renewal of registration the show cause notice
shall be served not later than thirty days before the expiration of the
registration. These proceedings shall be conducted in accordance
with chapter 1 of title 17 of this Code without regard to any criminal
prosecution or other proceeding. Proceedings to refuse renewal of
registration shall not abate the existing registration which shall remain
in effect pending the outcome of the administrative
hearing.
(2)
The director may suspend, without a notice to show cause, any
registration simultaneously with the institution of proceedings under
section 274 of this title, or where renewal of registration is refused, if
he finds that there is an imminent danger to the public health or safety
which warrants this action. The suspension shall continue in effect until
the conclusion of the proceedings, including judicial review thereof,
unless sooner withdrawn by the director or dissolved by a court of
competent jurisdiction. (P.L. No. 5-110.)
Source: 63 TTC 4 § 275,
modified.
§276. Same; records. Persons registered to
manufacture, distribute, or dispense controlled substances under this
chapter shall keep records and maintain inventories in conformance with
the record-keeping and inventory requirements of federal law and in
accordance with any rules or regulations adopted by the director pursuant
to the provisions of this chapter. (P.L. No. 5-110.)
Source: 63 TTC 4 § 276,
modified.
§277. Order forms for substances on schedules I or
II. Controlled substances in
schedules I and II shall be distributed by a registrant to another
registrant only pursuant to an order form. Compliance with the provisions
of federal law respecting order forms shall be deemed compliance with this
section. (P.L. No. 5-110.)
Source: 63 TTC 4 § 277,
modified.
(1)
Except when dispensed directly by a practitioner, other than a
pharmacy, to an ultimate user, no controlled substance in schedule II, may
be dispensed without the written prescription of a
practitioner.
(2)
In emergency situations, as defined by rule of the director,
schedule II drugs may be dispensed upon oral prescription of a
practitioner reduced promptly to writing and filled by the pharmacy.
Prescriptions shall be retained in conformity with the requirements
of section 276 of this title. No prescription for a schedule II
substance may be refilled.
(3)
Except when dispensed directly by a practitioner, other than a
pharmacy, to an ultimate user, a controlled substance included in
schedules III or IV which is a prescription drug, shall not be dispensed
without a written or oral prescription of a practitioner. The
prescription shall not be filled or refilled more than six months after
the date thereof or be refilled more than five times, unless renewed by
the practitioner.
(4)
A controlled substance included in schedule V shall not be
distributed or dispensed other than for a medical purpose.
(5)
No prescription for a controlled substance shall be filled or
refilled with more than a thirty day supply, based upon the dosage units
contained in the prescription. (P.L. No. 5-110.)
Source: 63 TTC 4 § 278,
modified.
Offenses and
Penalties
(1)
Except as authorized by this chapter, it shall be unlawful for any
person knowingly or intentionally:
(a) To manufacture, deliver or possess with
intent to manufacture, deliver or dispense, a controlled substance;
or
(b) To create, distribute, or possess with
intent to deliver, a counterfeit controlled substance.
(2)
Any person who violates paragraph (1) with respect
to:
(a) a substance classified in schedules I or II
which is a narcotic drug shall be sentenced to a term of imprisonment for
not more than ten years, a fine of not more than ten thousand dollars, or
both;
(b) any other controlled substance classified
in schedules I, II or III shall be sentenced to a term of imprisonment of
not more than five years, a fine of not more than five thousand dollars,
or both;
(c) a substance classified in schedule IV shall
be sentenced to a term of imprisonment for not more than two years, a fine
of not more than one thousand dollars, or both;
(d) a substance classified in schedule V shall
be sentenced to a term of imprisonment for not more than one year, a fine
of not more than one thousand dollars, or both.
(3)
Notwithstanding paragraph (2)(b) of this section, any person who
violates paragraph (1)(a) of this section by distributing not more than
one ounce of marihuana for no remuneration shall be treated as provided in
paragraph (3)(a) of section 292 of this title. (P.L. No.
5-110.)
Source: 63 TTC 4 § 291,
modified.
(1)
It is unlawful for any person knowingly or intentionally to possess
a controlled substance, unless such substance was obtained directly from,
or pursuant to, a valid prescription or order of a practitioner while
acting in the course of his professional practice, or except as otherwise
authorized by this chapter.
(2)
Any person who violates paragraph (1) with respect to any controlled
substance except marihuana shall be sentenced to a term of imprisonment
for not more than one year, a fine of not more than one thousand dollars,
or both.
(3)
Any person who violates paragraph (1) with respect to marihuana
shall be penalized as follows:
(a) Any person who possesses one ounce or less
shall be fined not more than fifty dollars;
(b) Any person possessing more than one ounce
but less than two and two-tenths pounds shall be sentenced to a term of
imprisonment of not more than three months, a fine of not more than five
hundred dollars, or both;
(c) Any person possessing two and two-tenths
pounds or more of marihuana shall be sentenced to a term of not more than
one year, a fine of not more than one thousand dollars, or both. The
possession of two and two-tenths pounds or more of marihuana by any person
shall constitute a rebuttable presumption of the crime of trafficking
under paragraph (b) of subsection (2) of section 291 of this title. (P.L.
No. 5-110.)
Source: 63 TTC 4 § 292,
modified.
§293. Commercial offenses.
(1)
It shall be unlawful for any person who is subject to the
requirements of subchapter III of this chapter:
(a) To distribute or dispense a controlled
substance not authorized by his registration to another registrant or
other authorized person;
(b) To manufacture, distribute, or dispense a
controlled substance not authorized by his registration to another
registrant or other authorized person;
(c) To refuse or fail to make, keep or furnish
any record, notification, order form, statement, invoice or information
required under this chapter; or
(d) To refuse an entry into any premises for
any inspection authorized by this chapter;
(e) To knowingly keep or maintain any store,
shop, warehouse, dwelling house, building, vehicle, boat, aircraft, or any
other structure or place whatever which is resorted to by persons using
controlled substances, or which is used for the keeping or selling of the
same in violation of this chapter.
(2)
Any person who violates this section is punishable by imprisonment
for not more than five years, or a fine of not more than one thousand
dollars, or both. (P.L. No. 5-110.)
Source: 63 TTC 4 § 293,
modified.
§294. Fraudulent practices.
(1)
It shall be unlawful for any person knowingly or
intentionally:
(a) To distribute a controlled substance
classified in schedules I or II, in the course of his legitimate business,
if that person is a registrant, except pursuant to an order form as
required by section 277 of this title;
(b) To use in the course of the manufacture or
distribution of a controlled substance a registration number which is
fictitious, revoked, suspended or issued to another
person;
(c) To acquire or obtain possession of a
controlled substance by misrepresentation, fraud, forgery, deception or
subterfuge;
(d) To furnish false or fraudulent material
information in, or omit any material information from, any application,
report, or other document required to be kept or filed under this chapter,
or any record required to be kept by this chapter;
(e) To make, distribute, or possess any punch,
die, plate, stone or other thing designed to print, imprint, or reproduce
the trademark, trade name, or other identifying mark, imprint, or device
of another or any likeness of any of the foregoing upon any drug or
container of labeling thereof so as to render such drug a counterfeit
controlled substance.
(2)
Any person who violates this section is punishable by imprisonment
for not more than five years, a fine of not more than one thousand
dollars, or both.(P.L. No. 5-110).
Source: 63 TTC 4 § 294,
modified.
§295. Attempts and conspiracies. Any person who attempts, endeavors or
conspires to commit any offense defined in this chapter is punishable by
imprisonment or fine or both which may not exceed the maximum punishment
prescribed for the offense, the commission of which was the object of the
attempt, endeavor or conspiracy. (P.L. No. 5-110.)
Source: 63 TTC 4 § 295,
modified.
§296. Penalties for violation of chapter to be in addition
to civil or administrative penalties. Any penalty imposed
for violation of this chapter shall be in addition to, and not in lieu of,
any civil or administrative penalty or sanction authorized by law. (P.L.
No. 5-110.)
Source: 63 TTC 4 § 296,
modified.
§297. Distribution to persons under eighteen.
Any person who is at least eighteen years of age who violates
subparagraph (a) of subsection (1) of section 291 of this title by
distributing a substance listed in schedules I and II which is a narcotic
drug to a person under eighteen years of age who is at least three years
his junior is punishable by a term of imprisonment of up to twice that
authorized by subparagraph (a) of subsection (1) of section 291 of this
title, by the fine authorized by subparagraph (a) of subsection (1) of
section 291 of this title, or both. Any person who is at least eighteen
years of age who violates subparagraph (a) of subsection (1) of section
291 of this title by distributing any other controlled substance listed in
schedules I, II, III and IV to a person under eighteen years of age who is
at least three years his junior is punishable by a term of imprisonment up
to twice that authorized in subparagraphs (b) or (c) of subsection (2) of
section 291 of this title, by the fine authorized by subparagraphs (b) or
(c) of subsection (2) of section 291 of this title, or both. (P.L. No.
5-110.)
Source: 63 TTC 4 § 297,
modified.
§298. Conditional discharge for first offense
possession.
(1)
Whenever any person who has not previously been convicted of any
offense under this chapter or under any statute of the United States or of
any state or territory relating to narcotic drugs, marihuana, or
stimulant, depressant, or hallucinogenic drugs, pleads guilty to or is
found guilty of possession of a controlled substance under paragraph (1)
of section 292 of this title the court, without entering a judgment of
guilt and with the consent of the accused, may defer further proceedings
and place him on probation upon terms and conditions. Upon violation
of a term or condition, the court may enter an adjudication of guilt and
proceed as otherwise provided. Upon fulfillment of the terms and
conditions, the court shall discharge such person and dismiss the
proceedings against him. Discharge and dismissal under this section
shall be without court adjudication of guilt and shall not be deemed a
conviction for purposes of disqualifications or disabilities imposed by
law upon conviction of a crime including the additional penalties imposed
for second or subsequent convictions under section 299 of this title.
Discharge and dismissal under this section may occur only once with
respect to any person.
(2)
Upon the dismissal of such person and discharge of the proceedings
against him under paragraph (1) of this section, such person may apply to
the court for an order to expunge from all official records (other than
the nonpublic records to be retained by the court solely for the purpose
of use by the courts in determining whether or not, in subsequent
proceedings, such person qualifies under this section) all recordation
relating to his arrest, indictment or information, trial, finding of
guilty, and dismissal and discharge pursuant to this section. If the
court determines after hearing that such person was dismissed and the
proceedings against him discharged, it shall enter such order. The
effect of such order shall be to restore such person, in the contemplation
of the law, to the status he occupied before such arrest or indictment or
information. No person as to whom such order has been entered shall be
held hereafter under any provisions of any law to be guilty of perjury or
otherwise giving a false statement by reason of his failures to recite or
acknowledge such arrest, or indictment or information, or trial in
response to any inquiry made of him for any purpose. (P.L. No.
5-110.)
Source: 63 TTC 4 § 298,
modified.
§299. Conviction by another jurisdiction not bar to
prosecution. If a violation of
this chapter is a violation of a federal law or the law of another state,
a conviction or acquittal under federal law or the law of another state
for the same act is not a bar to prosecution in the Trust Territory. (P.L.
No. 5-110.)
Source: 63 TTC 4 § 299,
modified.
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