21 U.s.c. 830

From the U.S. Code Online via GPO Access

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[Laws in effect as of January 3, 2005]

[Document not affected by Public Laws enacted between

January 3, 2005 and March 20, 2006]

[CITE: 21USC830]

TITLE 21--FOOD AND DRUGS

CHAPTER 13--DRUG ABUSE PREVENTION AND CONTROL

SUBCHAPTER I--CONTROL AND ENFORCEMENT

Part C--Registration of Manufacturers, Distributors, and Dispensers of

Controlled Substances

Sec. 830. Regulation of listed chemicals and certain machines

(a) Record of regulated transactions

(1) Each regulated person who engages in a regulated transaction

involving a listed chemical, a tableting machine, or an encapsulating

machine shall keep a record of the transaction for two years after the

date of the transaction.

(2) A record under this subsection shall be retrievable and shall

include the date of the regulated transaction, the identity of each

party to the regulated transaction, a statement of the quantity and form

of the listed chemical, a description of the tableting machine or

encapsulating machine, and a description of the method of transfer. Such

record shall be available for inspection and copying by the Attorney

General.

(3) It is the duty of each regulated person who engages in a

regulated transaction to identify each other party to the transaction.

It is the duty of such other party to present proof of identity to the

regulated person. The Attorney General shall specify by regulation the

types of documents and other evidence that constitute proof of identity

for purposes of this paragraph.

(b) Reports to Attorney General

(1) Each regulated person shall report to the Attorney General, in

such form and manner as the Attorney General shall prescribe by

regulation--

(A) any regulated transaction involving an extraordinary

quantity of a listed chemical, an uncommon method of payment or

delivery, or any other circumstance that the regulated person

believes may indicate that the listed chemical will be used in

violation of this subchapter;

(B) any proposed regulated transaction with a person whose

description or other identifying characteristic the Attorney General

furnishes in advance to the regulated person;

(C) any unusual or excessive loss or disappearance of a listed

chemical under the control of the regulated person; and

(D) any regulated transaction in a tableting machine or an

encapsulating machine.

Each report under subparagraph (A) shall be made at the earliest

practicable opportunity after the regulated person becomes aware of the

circumstance involved. A regulated person may not complete a transaction

with a person whose description or identifying characteristic is

furnished to the regulated person under subparagraph (B) unless the

transaction is approved by the Attorney General. The Attorney General

shall make available to regulated persons guidance documents describing

transactions and circumstances for which reports are required under

subparagraph (A) and subparagraph (C).

(2) A regulated person that manufactures a listed chemical shall

report annually to the Attorney General, in such form and manner and

containing such specific data as the Attorney General shall prescribe by

regulation, information concerning listed chemicals manufactured by the

person. The requirement of the preceding sentence shall not apply to the

manufacture of a drug product that is exempted under section

802(39)(A)(iv) of this title.

(3) Mail order reporting.--(A) As used in this paragraph:

(i) The term ``drug product'' means an active ingredient in

dosage form that has been approved or otherwise may be lawfully

marketed under the Food, Drug, and Cosmetic Act [21 U.S.C. 301 et

seq.] for distribution in the United States.

(ii) The term ``valid prescription'' means a prescription which

is issued for a legitimate medical purpose by an individual

practitioner licensed by law to administer and prescribe the drugs

concerned and acting in the usual course of the practitioner's

professional practice.

(B) Each regulated person who engages in a transaction with a

nonregulated person or who engages in an export transaction which--

(i) involves ephedrine, pseudoephedrine, or phenylpropanolamine

(including drug products containing these chemicals); and

(ii) uses or attempts to use the Postal Service or any private

or commercial carrier;

shall, on a monthly basis, submit a report of each such transaction

conducted during the previous month to the Attorney General in such

form, containing such data, and at such times as the Attorney General

shall establish by regulation.

(C) The data required for such reports shall include--

(i) the name of the purchaser;

(ii) the quantity and form of the ephedrine, pseudoephedrine, or

phenylpropanolamine purchased; and

(iii) the address to which such ephedrine, pseudoephedrine, or

phenylpropanolamine was sent.

(D) Except as provided in subparagraph (E), the following

distributions to a nonregulated person, and the following export

transactions, shall not be subject to the reporting requirement in

subparagraph (B):

(i) Distributions of sample packages of drug products when such

packages contain not more than two solid dosage units or the

equivalent of two dosage units in liquid form, not to exceed 10

milliliters of liquid per package, and not more than one package is

distributed to an individual or residential address in any 30-day

period.

(ii) Distributions of drug products by retail distributors that

may not include face-to-face transactions to the extent that such

distributions are consistent with the activities authorized for a

retail distributor as specified in section 802(46) of this title.

(iii) Distributions of drug products to a resident of a long

term care facility (as that term is defined in regulations

prescribed by the Attorney General) or distributions of drug

products to a long term care facility for dispensing to or for use

by a resident of that facility.

(iv) Distributions of drug products pursuant to a valid

prescription.

(v) Exports which have been reported to the Attorney General

pursuant to section 954 or 971 of this title or which are subject to

a waiver granted under section 971(e)(2) of this title.

(vi) Any quantity, method, or type of distribution or any

quantity, method, or type of distribution of a specific listed

chemical (including specific formulations or drug products) or of a

group of listed chemicals (including specific formulations or drug

products) which the Attorney General has excluded by regulation from

such reporting requirement on the basis that such reporting is not

necessary for the enforcement of this subchapter or subchapter II of

this chapter.

(E) The Attorney General may revoke any or all of the exemptions

listed in subparagraph (D) for an individual regulated person if he

finds that drug products distributed by the regulated person are being

used in violation of this subchapter or subchapter II of this chapter.

The regulated person shall be notified of the revocation, which will be

effective upon receipt by the person of such notice, as provided in

section 971(c)(1) of this title, and shall have the right to an

expedited hearing as provided in section 971(c)(2) of this title.

(c) Confidentiality of information obtained by Attorney General; non-

disclosure; exceptions

(1) Except as provided in paragraph (2), any information obtained by

the Attorney General under this section which is exempt from disclosure

under section 552(a) of title 5, by reason of section 552(b)(4) of such

title, is confidential and may not be disclosed to any person.

(2) Information referred to in paragraph (1) may be disclosed only--

(A) to an officer or employee of the United States engaged in

carrying out this subchapter, subchapter II of this chapter, or the

customs laws;

(B) when relevant in any investigation or proceeding for the

enforcement of this subchapter, subchapter II of this chapter, or

the customs laws;

(C) when necessary to comply with an obligation of the United

States under a treaty or other international agreement; or

(D) to a State or local official or employee in conjunction with

the enforcement of controlled substances laws or chemical control

laws.

(3) The Attorney General shall--

(A) take such action as may be necessary to prevent unauthorized

disclosure of information by any person to whom such information is

disclosed under paragraph (2); and

(B) issue guidelines that limit, to the maximum extent feasible,

the disclosure of proprietary business information, including the

names or identities of United States exporters of listed chemicals,

to any person to whom such information is disclosed under paragraph

(2).

(4) Any person who is aggrieved by a disclosure of information in

violation of this section may bring a civil action against the violator

for appropriate relief.

(5) Notwithstanding paragraph (4), a civil action may not be brought

under such paragraph against investigative or law enforcement personnel

of the Drug Enforcement Administration.

(Pub. L. 91-513, title II, Sec. 310, as added Pub. L. 95-633, title II,

Sec. 202(a), Nov. 10, 1978, 92 Stat. 3774; amended Pub. L. 100-690,

title VI, Sec. 6052(a), Nov. 18, 1988, 102 Stat. 4312; Pub. L. 103-200,

Secs. 2(c), 10, Dec. 17, 1993, 107 Stat. 2336, 2341; Pub. L. 104-237,

title II, Sec. 208, title IV, Sec. 402, Oct. 3, 1996, 110 Stat. 3104,

3111; Pub. L. 106-310, div. B, title XXXVI, Sec. 3652, Oct. 17, 2000,

114 Stat. 1239.)

References in Text

The Food, Drug, and Cosmetic Act, referred to in subsec.

(b)(3)(A)(i), probably means the Federal Food, Drug, and Cosmetic Act,

act June 25, 1938, ch. 675, 52 Stat. 1040, as amended, which is

classified generally to chapter 9 (Sec. 301 et seq.) of this title. For

complete classification of this Act to the Code, see section 301 of this

title and Tables.

This subchapter, referred to in subsec. (b)(3)(D)(vi), (E), was in

the original ``this title'', meaning title II of Pub. L. 91-513, Oct.

27, 1970, 84 Stat. 1242, as amended, and is popularly known as the

``Controlled Substances Act''. For complete classification of title II

to the Code, see second paragraph of Short Title note set out under

section 801 of this title and Tables.

Subchapter II of this chapter, referred to in subsecs.

(b)(3)(D)(iv), (E) and (c)(2)(A), (B), was in the original ``title

III'', meaning title III of Pub. L. 91-513, Oct. 27, 1970, 84 Stat.

1285, as amended. Part A of title III comprises subchapter II of this

chapter. For classification of Part B, consisting of sections 1101 to

1105 of title III, see Tables.

The customs laws, referred to in subsec. (c)(2)(A), (B), are

classified generally to Title 19, Customs Duties.

Amendments

2000--Subsec. (b)(3). Pub. L. 106-310 added subpars. (A), (D), and

(E), redesignated former subpars. (A) and (B) as (B) and (C),

respectively, and inserted ``or who engages in an export transaction''

after ``nonregulated person'' in introductory provisions of subpar. (B).

1996--Subsec. (a)(1). Pub. L. 104-237, Sec. 208, substituted ``for

two years after the date of the transaction.'' for the dash after

``record of the transaction'' and struck out subpars. (A) and (B) which

read as follows:

``(A) for 4 years after the date of the transaction, if the listed

chemical is a list I chemical or if the transaction involves a tableting

machine or an encapsulating machine; and

``(B) for 2 years after the date of the transaction, if the listed

chemical is a list II chemical.''

Subsec. (b)(3). Pub. L. 104-237, Sec. 402, added par. (3).

1993--Subsec. (a)(1). Pub. L. 103-200, Sec. 2(c)(1), substituted

``list I chemical'' for ``precursor chemical'' in subpar. (A) and ``a

list II chemical'' for ``an essential chemical'' in subpar. (B).

Subsec. (b). Pub. L. 103-200, Sec. 10, designated existing

provisions as par. (1), redesignated former pars. (1) to (4) as subpars.

(A) to (D), respectively, in concluding provisions, substituted

``subparagraph (A)'' for ``paragraph (1)'' in two places, ``subparagraph

(B)'' for ``paragraph (2)'', and ``subparagraph (C)'' for ``paragraph

(3)'', and added par. (2).

Subsec. (c)(2)(D). Pub. L. 103-200, Sec. 2(c)(2), substituted

``chemical control laws'' for ``precursor chemical laws''.

1988--Pub. L. 100-690 amended section generally, substituting

provisions relating to regulation of listed chemicals and certain

machines for provisions relating to reporting by any person who

distributes, sells, or imports any piperidine.

Effective Date of 1993 Amendment

Amendment by Pub. L. 103-200 effective on date that is 120 days

after Dec. 17, 1993, see section 11 of Pub. L. 103-200, set out as a

note under section 802 of this title.

Effective Date of 1988 Amendment

Amendment by Pub. L. 100-690 effective 120 days after Nov. 18, 1988,

see section 6061 of Pub. L. 100-690, set out as a note under section 802

of this title.

Effective Date; Time To Submit Piperidine Report; Required Information

Section 203(a) of title II of Pub. L. 95-633 provided that:

``(1) Except as provided under paragraph (2), the amendments made by

this title [enacting this section and amending sections 841 to 843 of

this title] shall take effect on the date of the enactment of this Act

[Nov. 10, 1978].

``(2) Any person required to submit a report under section 310(a)(1)

of the Controlled Substances Act [subsec. (a)(1) of this section]

respecting a distribution, sale, or importation of piperidine during the

90 days after the date of the enactment of this Act [Nov. 10, 1978] may

submit such report any time up to 97 days after such date of enactment.

``(3) Until otherwise provided by the Attorney General by

regulation, the information required to be reported by a person under

section 310(a)(1) of the Controlled Substances Act (as added by section

202(a)(2) of this title) [subsec. (a)(1) of this section] with respect

to the person's distribution, sale, or importation of piperidine shall--

``(A) be the information described in subparagraphs (A) and (B)

of such section, and

``(B) except as provided in paragraph (2) of this subsection, be

reported not later than seven days after the date of such

distribution, sale, or importation.''

Repeals

Pub. L. 96-359, Sec. 8(b), Sept. 26, 1980, 94 Stat. 1194, repealed

section 203(d) of Pub. L. 95-633, which had provided for the repeal of

this section effective Jan. 1, 1981.

Regulations for Piperidine Reporting

Section 203(b) of Pub. L. 95-633 required the Attorney General to

publish proposed interim regulations for piperidine reporting under

section 830(a) of this title not later than 30 days after enactment, and

final interim regulations not later than 75 days after enactment, such

final interim regulations to be effective on and after the ninety-first

day after enactment.

Report to President and Congress on Effectiveness of Title II of Pub. L.

95-633

Section 203(c) of Pub. L. 95-633 required the Attorney General to

analyze and evaluate the impact and effectiveness of the amendments made

by title II of Pub. L. 95-633, and report to the President and Congress

not later than Mar. 1, 1980.