§ 842.
(a)
Unlawful acts
It shall be unlawful for any person—
(1)
who is subject to the requirements of part C to distribute or dispense a controlled substance in violation of
section 829 of this title;
(2)
who is a registrant to distribute or dispense a controlled substance not authorized by his registration to another registrant or other authorized person or to manufacture a controlled substance not authorized by his registration;
(5)
to refuse or negligently fail to make, keep, or furnish any record, report, notification, declaration, order or order form, statement, invoice, or information required under this subchapter or subchapter II;
(6)
to refuse any entry into any premises or inspection authorized by this subchapter or subchapter II;
(7)
to remove, break, injure, or deface a seal placed upon controlled substances pursuant to section 824(f) or 881 of this title or to remove or dispose of substances so placed under seal;
(8)
to use, to his own advantage, or to reveal, other than to duly authorized officers or employees of the United States, or to the courts when relevant in any judicial proceeding under this subchapter or subchapter II, any information acquired in the course of an inspection authorized by this subchapter concerning any method or process which as a trade secret is entitled to protection, or to use to his own advantage or reveal (other than as authorized by
section 830 of this title) any information that is confidential under such section;
(9)
who is a regulated person to engage in a regulated transaction without obtaining the identification required by 830(a)(3) of this title.
(11)
to distribute a laboratory supply to a person who uses, or attempts to use, that laboratory supply to manufacture a controlled substance or a listed chemical, in violation of this subchapter or subchapter II, with reckless disregard for the illegal uses to which such a laboratory supply will be put;
(12)
(A)
to sell at retail a scheduled listed chemical product in violation of paragraph (1) of subsection (d) of such section, knowing at the time of the transaction involved (independent of consulting the logbook under subsection (e)(1)(A)(iii) of such section) that the transaction is a violation; or
(B)
to knowingly or recklessly sell at retail such a product in violation of paragraph (2) of such subsection (d);
(13)
who is a regulated seller to knowingly or recklessly sell at retail a scheduled listed chemical product in violation of subsection (e) of such section;
(14)
who is a regulated seller or an employee or agent of such seller to disclose, in violation of regulations under subparagraph (C) of
section 830(e)(1) of this title, information in logbooks under subparagraph (A)(iii) of such section, or to refuse to provide such a logbook to Federal, State, or local law enforcement authorities;
(15)
to distribute a scheduled listed chemical product to a regulated seller, or to a regulated person referred to in
section 830(b)(3)(B) of this title, unless such regulated seller or regulated person is, at the time of such distribution, currently registered with the Drug Enforcement Administration, or on the list of persons referred to under
section 830(e)(1)(B)(v) of this title;
(17)
in the case of a registered manufacturer or distributor of opioids, to fail to review the most recent information, directly related to the customers of the manufacturer or distributor, made available by the Attorney General in accordance with
section 827(f) of this title.
As used in paragraph (11), the term “laboratory supply” means a listed chemical or any chemical, substance, or item on a special surveillance list published by the Attorney General, which contains chemicals, products, materials, or equipment used in the manufacture of controlled substances and listed chemicals. For purposes of paragraph (11), there is a rebuttable presumption of reckless disregard at trial if the Attorney General notifies a firm in writing that a laboratory supply sold by the firm, or any other person or firm, has been used by a customer of the notified firm, or distributed further by that customer, for the unlawful production of controlled substances or listed chemicals a firm distributes and 2 weeks or more after the notification the notified firm distributes a laboratory supply to the customer. For purposes of paragraph (15), if the distributor is temporarily unable to access the list of persons referred to under
section 830(e)(1)(B)(v) of this title, the distributor may rely on a written, faxed, or electronic copy of a certificate of self-certification submitted by the regulated seller or regulated person, provided the distributor confirms within 7 business days of the distribution that such regulated seller or regulated person is on the list referred to under
section 830(e)(1)(B)(v) of this title.
(b)
Manufacture
It shall be unlawful for any person who is a registrant to manufacture a controlled substance in schedule I or II, or ephedrine, pseudoephedrine, or phenylpropanolamine or any of the salts, optical isomers, or salts of optical isomers of such chemical, which is—
([Pub. L. 91–513, title II, § 402], Oct. 27, 1970, [84 Stat. 1262]; [Pub. L. 95–633, title II, § 202(b)(1)], (2), Nov. 10, 1978, [92 Stat. 3776]; [Pub. L. 100–690, title VI, § 6056], Nov. 18, 1988, [102 Stat. 4318]; [Pub. L. 104–237, title II, § 205], Oct. 3, 1996, [110 Stat. 3103]; [Pub. L. 105–277, div. A, § 101(b) [title I, § 117]], Oct. 21, 1998, [112 Stat. 2681–50], 2681–68; [Pub. L. 107–273, div. B, title IV, § 4002(b)(16)], (d)(2)(B), Nov. 2, 2002, [116 Stat. 1808], 1809; [Pub. L. 109–177, title VII], §§ 711(f)(1)(A), (2), 714, Mar. 9, 2006, [120 Stat. 262–264]; [Pub. L. 111–268], §§ 4, 5, Oct. 12, 2010, [124 Stat. 2847], 2848; [Pub. L. 113–260, § 3(c)], Dec. 18, 2014, [128 Stat. 2931]; [Pub. L. 115–271, title III, § 3273(c)], Oct. 24, 2018, [132 Stat. 3953].)