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Code of Federal Regulations Title 21. Food and Drugs § 21.207.37 What restrictions pertain to the use of the NDC?

Current as of January 02, 2025 | Updated by Findlaw Staff

(a) A product may be deemed to be misbranded if an NDC is used:

(1) To represent a different drug than the drug for which the NDC has been assigned, as described in § 207.33;

(2) To denote or imply FDA approval of a drug;  or

(3) On products that are not subject to parts 207, 607 of this chapter, or 1271 of this chapter, such as dietary supplements and medical devices.

(b) If marketing is resumed for a discontinued drug, and no changes have been made to the drug that would require a new NDC under § 207.35, the drug must have the same NDC that was assigned to it as described in § 207.33, before marketing was discontinued.

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Cite this article: FindLaw.com - Code of Federal Regulations Title 21. Food and Drugs § 21.207.37 What restrictions pertain to the use of the NDC? - last updated January 02, 2025 | https://codes.findlaw.com/cfr/title-21-food-and-drugs/cfr-sect-21-207-37/

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