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21 U.S.C. § 335c — Authority to withdraw approval of abbre-

Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 335c — Authority to withdraw approval of abbre-

Page 76 TITLE 21—FOOD AND DRUGS § 335c (1) $250,000, or (2) one-half of the penalty so imposed and collected, whichever is less. The decision of the Secretary on such award shall not be reviewable. (June 25, 1938, ch. 675, § 307, as added Pub. L. 102–282, § 3, May 13, 1992, 106 Stat. 159; amended Pub. L. 103–80, § 3(g), Aug. 13, 1993, 107 Stat. 776.) Editorial Notes PRIOR PROVISIONS A prior section 307 of act June 25, 1938, was renum- bered section 310 and is classified to section 337 of this title. AMENDMENTS 1993—Subsec. (b)(3)(A). Pub. L. 103–80 made technical amendment to reference to May 13, 1992, to reflect cor- rection of corresponding provision of original act. Statutory Notes and Related Subsidiaries CONSTRUCTION This section not to preclude any other civil, criminal, or administrative remedy provided under Federal or State law, including any private right of action against any person for the same action subject to any action or civil penalty under an amendment made by Pub. L. 102–282, see section 7 of Pub. L. 102–282, set out as a note under section 335a of this title. § 335c. Authority to withdraw approval of abbre- viated drug applications (a) In general The Secretary— (1) shall withdraw approval of an abbre- viated drug application if the Secretary finds that the approval was obtained, expedited, or otherwise facilitated through bribery, pay- ment of an illegal gratuity, or fraud or mate- rial false statement, and (2) may withdraw approval of an abbreviated drug application if the Secretary finds that the applicant has repeatedly demonstrated a lack of ability to produce the drug for which the application was submitted in accordance with the formulations or manufacturing prac- tice set forth in the abbreviated drug applica- t

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Source file: Laws/federal/codes/united-states-code-2024/title-21/section-335c-authority-to-withdraw-approval-of-abbre--edea97b809.md
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Page 76 TITLE 21—FOOD AND DRUGS § 335c (1) $250,000, or (2) one-half of the penalty so imposed and collected, whichever is less. The decision of the Secretary on such award shall not be reviewable. (June 25, 1938, ch. 675, § 307, as added Pub. L. 102–282, § 3, May 13, 1992, 106 Stat. 159; amended Pub. L. 103–80, § 3(g), Aug. 13, 1993, 107 Stat. 776.) Editorial Notes PRIOR PROVISIONS A prior section 307 of act June 25, 1938, was renum- bered section 310 and is classified to section 337 of this title. AMENDMENTS 1993—Subsec. (b)(3)(A). Pub. L. 103–80 made technical amendment to reference to May 13, 1992, to reflect cor- rection of corresponding provision of original act. Statutory Notes and Related Subsidiaries CONSTRUCTION This section not to preclude any other civil, criminal, or administrative remedy provided under Federal or State law, including any private right of action against any person for the same action subject to any action or civil penalty under an amendment made by Pub. L. 102–282, see section 7 of Pub. L. 102–282, set out as a note under section 335a of this title. § 335c. Authority to withdraw approval of abbre- viated drug applications (a) In general The Secretary— (1) shall withdraw approval of an abbre- viated drug application if the Secretary finds that the approval was obtained, expedited, or otherwise facilitated through bribery, pay- ment of an illegal gratuity, or fraud or mate- rial false statement, and (2) may withdraw approval of an abbreviated drug application if the Secretary finds that the applicant has repeatedly demonstrated a lack of ability to produce the drug for which the application was submitted in accordance with the formulations or manufacturing prac- tice set forth in the abbreviated drug applica- tion and has introduced, or attempted to in- troduce, such adulterated or misbranded drug into commerce. (b) Procedure The Secretary may not take any action under subsection (a) with respect to any person unless the Secretary has issued an order for such ac- tion made on the record after opportunity for an agency hearing on disputed issues of material fact. In the course of any investigation or hear- ing under this subsection, the Secretary may ad- minister oaths and affirmations, examine wit- nesses, receive evidence, and issue subpoenas re- quiring the attendance and testimony of wit- nesses and the production of evidence that re- lates to the matter under investigation. (c) Applicability Subsection (a) shall apply with respect to of- fenses or acts regardless of when such offenses or acts occurred. (d) Judicial review Any person that is the subject of an adverse decision under subsection (a) may obtain a re- view of such decision by the United States Court of Appeals for the District of Columbia or for the circuit in which the person resides, by filing in such court (within 60 days following the date the person is notified of the Secretary’s deci- sion) a petition requesting that the decision be modified or set aside. (June 25, 1938, ch. 675, § 308, as added Pub. L. 102–282, § 4, May 13, 1992, 106 Stat. 160.) Statutory Notes and Related Subsidiaries CONSTRUCTION This section not to preclude any other civil, criminal, or administrative remedy provided under Federal or State law, including any private right of action against any person for the same action subject to any action or civil penalty under an amendment made by Pub. L. 102–282, see section 7 of Pub. L. 102–282, set out as a note under section 335a of this title. § 336. Report of minor violations Nothing in this chapter shall be construed as requiring the Secretary to report for prosecu- tion, or for the institution of libel or injunction proceedings, minor violations of this chapter whenever he believes that the public interest will be adequately served by a suitable written notice or warning. (June 25, 1938, ch. 675, § 309, formerly § 306, 52 Stat. 1045; renumbered § 309, Pub. L. 102–282, § 2, May 13, 1992, 106 Stat. 150.) Executive Documents TRANSFER OF FUNCTIONS For transfer of functions of Federal Security Admin- istrator to Secretary of Health, Education, and Welfare [now Health and Human Services], and of Food and Drug Administration in the Department of Agriculture to Federal Security Agency, see notes set out under section 321 of this title. § 337. Proceedings in name of United States; pro- vision as to subpoenas (a) Except as provided in subsection (b), all such proceedings for the enforcement, or to re- strain violations, of this chapter shall be by and in the name of the United States. Subpoenas for witnesses who are required to attend a court of the United States, in any district, may run into any other district in any proceeding under this section. (b)(1) A State may bring in its own name and within its jurisdiction proceedings for the civil enforcement, or to restrain violations, of section 341, 343(b), 343(c), 343(d), 343(e), 343(f), 343(g), 343(h), 343(i), 343(k), 343(q), or 343(r) of this title if the food that is the subject of the proceedings is located in the State. (2) No proceeding may be commenced by a State under paragraph (1)— (A) before 30 days after the State has given notice to the Secretary that the State intends to bring such proceeding, (B) before 90 days after the State has given notice to the Secretary of such intent if the Secretary has, within such 30 days, com- menced an informal or formal enforcement ac- tion pertaining to the food which would be the subject of such proceeding, or

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Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 335c — Authority to withdraw approval of abbreviated drug applications

**(a) In general** The Secretary— (1) shall withdraw approval of an abbreviated drug application if the Secretary finds that the approval was obtained, expedited, or otherwise facilitated through bribery, payment of an illegal gratuity, or fraud or material false statement, and (2) may withdraw approval of an abbreviated drug application if the Secretary finds that the applicant has repeatedly demonstrated a lack of ability to produce the drug for which the application was submitted in accordance with the formulations or manufacturing practice set forth in the abbreviated drug application and has introduced, or attempted to introduce, such adulterated or misbranded drug into commerce. **(b) Procedure** The Secretary may not take any action under subsection (a) with respect to any person unless the Secretary has issued an order for such action made on the record after opportunity for an agency hearing on disputed issues of material fact. In the course of any investigation or hearing under this subsection, the Secretary may administer oaths and affirmations, examine witnesses, receive evidence, and issue subpoenas requiring the attendance and testimony of witnesses and the production of evidence that relates to the matter under investigation. **(c) Applicability** Subsection (a) shall apply with respect to offenses or acts regardless of when such offenses or acts occurred. **(d) Judicial review** Any person that is the subject of an adverse decision under subsection (a) may obtain a review of such decision by the United States Court of Appeals for the District of Columbia or for the circuit in which the person resides, by filing in such court (within 60 days following the date the person is notified of the Secretary’s decision) a petition requesting that the decision

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