FEDERAL · 21 U.S.C. · Chapter 9

Prompt reports of marketing status

21 U.S.C. § 356i
Title21Food and Drugs
Chapter9 — FEDERAL FOOD, DRUG, AND COSMETIC ACT
SubchapterV
PartA
Current throughPub. L. 119-99

This text of 21 U.S.C. § 356i (Prompt reports of marketing status) is published on Counsel Stack Legal Research, covering United States primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
21 U.S.C. § 356i.

Text

(a)Notification of withdrawal The holder of an application approved under subsection (c) or (j) of section 355 of this title or subsection (a) or (k) of section 262 of title 42 shall notify the Secretary in writing 180 days prior to withdrawing the approved drug from sale, or if 180 days is not practicable as soon as practicable but not later than the date of withdrawal. The holder shall include with such notice the—
(1)National Drug Code;
(2)identity of the drug by established name (or, in the case of a biological product, the proper name) and by proprietary name, if any;
(3)new drug application number, abbreviated application number, or biologics license application number;
(4)strength of the drug;
(5)date on which the drug is expected to no longer be available for sale; and
(6)re

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Related

§ 355
21 U.S.C. § 355
§ 262
42 U.S.C. § 262
§ 262
21 U.S.C. § 262

Source Credit

History

(June 25, 1938, ch. 675, §506I, as added Pub. L. 115–52, title VIII, §804, Aug. 18, 2017, 131 Stat. 1071; amended Pub. L. 117–328, div. FF, title III, §3201, Dec. 29, 2022, 136 Stat. 5808.)

Editorial Notes

Editorial Notes

Amendments
2022—Subsec. (a). Pub. L. 117–328, §3201(a)(1)(A), substituted "The holder of an application approved under subsection (c) or (j) of section 355 of this title or subsection (a) or (k) of section 262 of title 42" for "The holder of an application approved under subsection (c) or (j) of section 355 of this title" in introductory provisions.
Subsec. (a)(2). Pub. L. 117–328, §3201(a)(1)(B), substituted "established name (or, in the case of a biological product, the proper name)" for "established name".
Subsec. (a)(3). Pub. L. 117–328, §3201(a)(1)(C), substituted ", abbreviated application number, or biologics license application number" for "or abbreviated application number".
Subsec. (b). Pub. L. 117–328, §3201(a)(2)(A), substituted "The holder of an application approved under subsection (c) or (j) of section 355 of this title or subsection (a) or (k) of section 262 of title 42" for "The holder of an application approved under subsection (c) or (j)" in introductory provisions.
Subsec. (b)(1). Pub. L. 117–328, §3201(a)(2)(B), substituted "established name (or, in the case of a biological product, the proper name)" for "established name".
Subsec. (b)(2). Pub. L. 117–328, §3201(a)(2)(C), substituted ", abbreviated application number, or biologics license application number" for "or abbreviated application number".
Subsec. (c). Pub. L. 117–328, §3201(b), amended subsec. (c) generally. Prior to amendment, subsec. (c) related to an additional one-time report to be done within 180 days of Aug. 18, 2017.
Subsec. (d). Pub. L. 117–328, §3201(c)(1), added subsec. (d) and struck out former subsec. (d). Prior to amendment, text read as follows: "If a holder of an approved application fails to submit the information required under subsection (a), (b), or (c), the Secretary may move the application holder's drugs from the active section of the list published under subsection 355(j)(7)(A) of this title to the discontinued section of the list, except that the Secretary shall remove from the list in accordance with subsection 355(j)(7)(C) of this title drugs the Secretary determines have been withdrawn from sale for reasons of safety of effectiveness."
Subsec. (e). Pub. L. 117–328, §3201(d), substituted "section 355(j)(7)(A) of this title" for "subsection 355(j)(7)(A) of this title" and "section 355(j)(7)(C) of this title" for "subsection 355(j)(7)(C) of this title".
Pub. L. 117–328, §3201(c)(2), inserted "The Secretary shall update the list published under section 262(k)(9)(A) of title 42 based on information provided under subsections (a), (b), and (c) by identifying as discontinued biological products that are not available for sale, except that biological products for which the license has been revoked or suspended for safety, purity, or potency reasons shall be removed from the list in accordance with section 262(k)(9)(B) of title 42." before "The Secretary shall make monthly updates" and substituted "monthly updates to the lists referred to in the preceding sentences" for "monthly updates to the list" and "and shall update such lists based on" for "and shall update the list based on".

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Bluebook (online)
21 U.S.C. § 356i, Counsel Stack Legal Research, https://law.counselstack.com/usc/21/356i.