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21 U.S.C. § 952 — Importation of controlled substances
Federal law — U.S. Code and appendices · legal_authorities
Page 893
TITLE 21—FOOD AND DRUGS
§ 952
ternal Revenue Code of 1986 [formerly I.R.C. 1954, sec-
tion 4722 of Title 26] as a prerequisite to issuance of
such a license, shall be superseded by a requirement of
actual registration (as distinguished from provisional
registration) as a manufacturer of that class of drug
under section 303(a) of title II [section 823(a) of this
title].
‘‘(C) On and after the effective date of the repeal of
such section 4722 [section 4722 of title 26] by section
1101(b)(3) of this title, but prior to the date specified in
subparagraph (B) of this paragraph, the requirement of
registration under such section 4722 [section 4722 of
title 26] as a prerequisite of a manufacturer’s license
under the Narcotics Manufacturing Act of 1960 [sec-
tions 501 to 517 of this title] shall be superseded by a re-
quirement of either (i) actual registration as a manu-
facturer under section 303 of title II [section 823 of this
title] or (ii) provisional registration (by virtue of a pre-
existing registration under such section 4722) under sec-
tion 703 of title II [set out as a note under section 822
of this title].’’
SHORT TITLE
Pub. L. 91–513, title III, § 1000, Oct. 27, 1970, 84 Stat.
1285, provided that: ‘‘This title [enacting this sub-
chapter, amending sections 162 and 967 of this title, sec-
tion 4251 of Title 18, Crimes and Criminal Procedure,
section 1584 of Title 19, Customs Duties, sections 4901,
4905, 6808, 7012, 7103, 7326, 7607, 7609, 7641, 7651, and 7655
of Title 26, Internal Revenue Code, section 2901 of Title
28, Judiciary and Judicial Procedure, sections 529d,
529e, and 529f of former Title 31, Money and Finance,
section 304m of former Title 40, Public Buildings, Prop-
erty, and Works, section 3411 of Title 42, The Public
He
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Page 893
TITLE 21—FOOD AND DRUGS
§ 952
ternal Revenue Code of 1986 [formerly I.R.C. 1954, sec-
tion 4722 of Title 26] as a prerequisite to issuance of
such a license, shall be superseded by a requirement of
actual registration (as distinguished from provisional
registration) as a manufacturer of that class of drug
under section 303(a) of title II [section 823(a) of this
title].
‘‘(C) On and after the effective date of the repeal of
such section 4722 [section 4722 of title 26] by section
1101(b)(3) of this title, but prior to the date specified in
subparagraph (B) of this paragraph, the requirement of
registration under such section 4722 [section 4722 of
title 26] as a prerequisite of a manufacturer’s license
under the Narcotics Manufacturing Act of 1960 [sec-
tions 501 to 517 of this title] shall be superseded by a re-
quirement of either (i) actual registration as a manu-
facturer under section 303 of title II [section 823 of this
title] or (ii) provisional registration (by virtue of a pre-
existing registration under such section 4722) under sec-
tion 703 of title II [set out as a note under section 822
of this title].’’
SHORT TITLE
Pub. L. 91–513, title III, § 1000, Oct. 27, 1970, 84 Stat.
1285, provided that: ‘‘This title [enacting this sub-
chapter, amending sections 162 and 967 of this title, sec-
tion 4251 of Title 18, Crimes and Criminal Procedure,
section 1584 of Title 19, Customs Duties, sections 4901,
4905, 6808, 7012, 7103, 7326, 7607, 7609, 7641, 7651, and 7655
of Title 26, Internal Revenue Code, section 2901 of Title
28, Judiciary and Judicial Procedure, sections 529d,
529e, and 529f of former Title 31, Money and Finance,
section 304m of former Title 40, Public Buildings, Prop-
erty, and Works, section 3411 of Title 42, The Public
Health and Welfare, section 239a of former Title 46,
Shipping, and section 787 of former Title 49, Transpor-
tation, repealing sections 171 to 174, 176 to 185, 188 to
188n, 191 to 193, 197, 198, 199, and 501 to 517 of this title,
sections 1401 to 1407, and 3616 of Title 18, sections 4701
to 4707, 4711 to 4716, 4721 to 4726, 4731 to 4736, 4741 to 4746,
4751 to 4757, 4761, 4762, 4771 to 4776, 7237, 7238, and 7491 of
Title 26, sections 529a and 529g of former Title 31, sec-
tion 1421m of Title 48, Territories and Insular Posses-
sions, and enacting provisions set out as notes under
this section and sections 171 and 957 of this title] may
be cited as the ‘Controlled Substances Import and Ex-
port Act’.’’
RULES AND REGULATIONS
Pub. L. 91–513, title III, § 1105(d), Oct. 27, 1970, 84 Stat.
1296, provided: ‘‘Any orders, rules and regulations
which have been promulgated under any law affected
by this title [see Short Title note above] and which are
in effect on the day preceding enactment of this title
[Oct. 27, 1970] shall continue in effect until modified,
superseded, or repealed.’’
§ 952. Importation of controlled substances
(a) Controlled substances in schedule I or II and
narcotic drugs in schedule III, IV, or V; ex-
ceptions
It shall be unlawful to import into the cus-
toms territory of the United States from any
place outside thereof (but within the United
States), or to import into the United States
from any place outside thereof, any controlled
substance in schedule I or II of subchapter I, or
any narcotic drug in schedule III, IV, or V of
subchapter I, or ephedrine, pseudoephedrine, or
phenylpropanolamine, except that—
(1) such amounts of crude opium, poppy
straw, concentrate of poppy straw, and coca
leaves, and of ephedrine, pseudoephedrine, and
phenylpropanolamine, as the Attorney Gen-
eral finds to be necessary to provide for med-
ical, scientific, or other legitimate purposes,
and
(2) such amounts of any controlled substance
in schedule I or II or any narcotic drug in
schedule III, IV, or V that the Attorney Gen-
eral finds to be necessary to provide for the
medical, scientific, or other legitimate needs
of the United States—
(A) during an emergency in which domes-
tic supplies of such substance or drug are
found by the Attorney General to be inad-
equate,
(B) in any case in which the Attorney Gen-
eral finds that competition among domestic
manufacturers of the controlled substance is
inadequate and will not be rendered ade-
quate by the registration of additional man-
ufacturers under section 823 of this title, or
(C) in any case in which the Attorney Gen-
eral finds that such controlled substance is
in limited quantities exclusively for sci-
entific, analytical, or research uses,
may be so imported under such regulations as
the Attorney General shall prescribe. No crude
opium may be so imported for the purpose of
manufacturing heroin or smoking opium.
(b) Nonnarcotic controlled substances in sched-
ule III, IV, or V
It shall be unlawful to import into the cus-
toms territory of the United States from any
place outside thereof (but within the United
States), or to import into the United States
from
any
place
outside
thereof,
any
non-
narcotic controlled substance in schedule III,
IV, or V, unless such nonnarcotic controlled sub-
stance—
(1) is imported for medical, scientific, or
other legitimate uses, and
(2) is imported pursuant to such notification,
or declaration, or in the case of any nonnar-
cotic controlled substance in schedule III,
such import permit, notification, or declara-
tion, as the Attorney General may by regula-
tion prescribe, except that if a nonnarcotic
controlled substance in schedule IV or V is
also listed in schedule I or II of the Conven-
tion on Psychotropic Substances it shall be
imported pursuant to such import permit re-
quirements, prescribed by regulation of the
Attorney General, as are required by the Con-
vention.
(c) Coca leaves
In addition to the amount of coca leaves au-
thorized to be imported into the United States
under subsection (a), the Attorney General may
permit the importation of additional amounts of
coca leaves. All cocaine and ecgonine (and all
salts, derivatives, and preparations from which
cocaine or ecgonine may be synthesized or
made) contained in such additional amounts of
coca leaves imported under this subsection shall
be destroyed under the supervision of an author-
ized representative of the Attorney General.
(d) Application for increased importation of
ephedrine,
pseudoephedrine,
or
phenyl-
propanolamine
(1) With respect to a registrant under section
958 of this title who is authorized under sub-
section
(a)(1)
to
import
ephedrine,
pseudoephedrine, or phenylpropanolamine, at
any time during the year the registrant may
Page 894
TITLE 21—FOOD AND DRUGS
§ 953
apply for an increase in the amount of such
chemical that the registrant is authorized to
import, and the Attorney General may approve
the application if the Attorney General deter-
mines that the approval is necessary to provide
for medical, scientific, or other legitimate pur-
poses regarding the chemical.
(2) With respect to the application under para-
graph (1):
(A) Not later than 60 days after receiving the
application, the Attorney General shall ap-
prove or deny the application.
(B) In approving the application, the Attor-
ney General shall specify the period of time
for which the approval is in effect, or shall
provide that the approval is effective until the
registrant involved is notified in writing by
the Attorney General that the approval is ter-
minated.
(C) If the Attorney General does not approve
or deny the application before the expiration
of the 60-day period under subparagraph (A),
the application is deemed to be approved, and
such approval remains in effect until the At-
torney General notifies the registrant in writ-
ing that the approval is terminated.
(e) Reference to ephedrine, pseudoephedrine, or
phenylpropanolamine
Each reference in this section to ephedrine,
pseudoephedrine, or phenylpropanolamine in-
cludes each of the salts, optical isomers, and
salts of optical isomers of such chemical.
(Pub. L. 91–513, title III, § 1002, Oct. 27, 1970, 84
Stat. 1285; Pub. L. 95–633, title I, § 105, Nov. 10,
1978, 92 Stat. 3772; Pub. L. 98–473, title II,
§§ 519–521, Oct. 12, 1984, 98 Stat. 2075; Pub. L.
109–177, title VII, § 715, Mar. 9, 2006, 120 Stat. 264.)
Editorial Notes
REFERENCES IN TEXT
Schedules I, II, III, IV, and V, referred to in subsecs.
(a) and (b), are set out in section 812(c) of this title.
AMENDMENTS
2006—Subsec. (a). Pub. L. 109–177, § 715(1)(A), inserted
‘‘or ephedrine, pseudoephedrine, or phenylpropanola-
mine,’’ after ‘‘schedule III, IV, or V of subchapter I,’’ in
introductory provisions.
Subsec. (a)(1). Pub. L. 109–177, § 715(1)(B), inserted
‘‘, and of ephedrine, pseudoephedrine, and phenyl-
propanolamine,’’ after ‘‘coca leaves’’.
Subsecs. (d), (e). Pub. L. 109–177, § 715(2), added sub-
secs. (d) and (e).
1984—Subsec. (a)(1). Pub. L. 98–473, § 519, amended par.
(1) generally, inserting references to poppy straw and
concentrate of poppy straw.
Subsec. (a)(2)(C). Pub. L. 98–473, § 520, added subpar.
(C).
Subsec. (b)(2). Pub. L. 98–473, § 521, substituted ‘‘is im-
ported pursuant to such notification, or declaration, or
in the case of any nonnarcotic controlled substance in
schedule III, such import permit, notification, or dec-
laration, as the Attorney General may by regulation
prescribe, except that if a nonnarcotic controlled sub-
stance in schedule IV or V is also listed in schedule I
or II of the Convention on Psychotropic Substances it
shall be imported pursuant to such import permit re-
quirements, prescribed by regulation of the Attorney
General, as are required by the Convention’’ for ‘‘is im-
ported pursuant to such notification or declaration re-
quirements as the Attorney General may by regulation
prescribe, except that if a nonnarcotic controlled sub-
stance in schedule III, IV, or V is also listed in schedule
I or II of the Convention on Psychotropic Substances it
shall be imported pursuant to such import permit re-
quirements, prescribed by regulation of the Attorney
General, as are required by the Convention’’.
1978—Subsec. (b)(2). Pub. L. 95–633 inserted provision
relating to exception for nonnarcotic controlled sub-
stances listed in schedule I or II of the Convention on
Psychotropic Substances.
Statutory Notes and Related Subsidiaries
EFFECTIVE DATE OF 1978 AMENDMENT
Amendment by Pub. L. 95–633 effective on date the
Convention on Psychotropic Substances enters into
force in the United States [July 15, 1980], see section 112
of Pub. L. 95–633, set out as an Effective Date note
under section 801a of this title.
EFFECTIVE DATE
Section effective on first day of seventh calendar
month that begins after Oct. 26, 1970, see 1105(a) of Pub.
L. 91–513, set out as a under section 951 of this title.
§ 953. Exportation of controlled substances
(a) Narcotic drugs in schedule I, II, III, or IV
It shall be unlawful to export from the United
States any narcotic drug in schedule I, II, III, or
IV unless—
(1) it is exported to a country which is a
party to—
(A) the International Opium Convention of
1912 for the Suppression of the Abuses of
Opium, Morphine, Cocaine, and Derivative
Drugs, or to the International Opium Con-
vention signed at Geneva on February 19,
1925; or
(B) the Convention for Limiting the Manu-
facture and Regulating the Distribution of
Narcotic Drugs concluded at Geneva, July
13, 1931, as amended by the protocol signed
at Lake Success on December 11, 1946, and
the protocol bringing under international
control drugs outside the scope of the con-
vention of July 13, 1931, for limiting the
manufacture and regulating the distribution
of narcotic drugs (as amended by the pro-
tocol signed at Lake Success on December
11, 1946), signed at Paris, November 19, 1948;
or
(C) the Single Convention on Narcotic
Drugs, 1961, signed at New York, March 30,
1961;
(2) such country has instituted and main-
tains, in conformity with the conventions to
which it is a party, a system for the control of
imports of narcotic drugs which the Attorney
General deems adequate;
(3) the narcotic drug is consigned to a holder
of such permits or licenses as may be required
under the laws of the country of import, and a
permit or license to import such drug has been
issued by the country of import;
(4) substantial evidence is furnished to the
Attorney General by the exporter that (A) the
narcotic drug is to be applied exclusively to
medical or scientific uses within the country
of import, and (B) there is an actual need for
the narcotic drug for medical or scientific uses
within such country; and
(5) a permit to export the narcotic drug in
each instance has been issued by the Attorney
General.
Cross-references
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Federal law — U.S. Code and appendices · legal_authorities
**(a) Controlled substances in schedule I or II and narcotic drugs in schedule III, IV, or V; exceptions** It shall be unlawful to import into the customs territory of the United States from any place outside thereof (but within the United States), or to import into the United States from any place outside thereof, any controlled substance in schedule I or II of subchapter I, or any narcotic drug in schedule III, IV, or V of subchapter I, or ephedrine, pseudoephedrine, or phenylpropanolamine, except that—
(1) such amounts of crude opium, poppy straw, concentrate of poppy straw, and coca leaves, and of ephedrine, pseudoephedrine, and phenylpropanolamine, as the Attorney General finds to be necessary to provide for medical, scientific, or other legitimate purposes, and
(2) such amounts of any controlled substance in schedule I or II or any narcotic drug in schedule III, IV, or V that the Attorney General finds to be necessary to provide for the medical, scientific, or other legitimate needs of the United States—
(A) during an emergency in which domestic supplies of such substance or drug are found by the Attorney General to be inadequate,
(B) in any case in which the Attorney General finds that competition among domestic manufacturers of the controlled substance is inadequate and will not be rendered adequate by the registration of additional manufacturers under [section 823 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section823&num=0&edition=prelim), or
(C) in any case in which the Attorney General finds that such controlled substance is in limited quantities exclusively for scientific, analytical, or research uses,
may be so imported under such regulations as the Attorney General shall prescribe. No crude opium may be s
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