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Code of Federal Regulations Title 21. Food and Drugs § 21.207.54 What listing information must a registrant submit for a drug that it salvages?

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

A registrant who also relabels or repacks a drug that it salvages must list the drug it relabels or repacks in accordance with § 207.53 rather than in accordance with this section. A registrant who performs only salvaging with respect to a drug must provide the following listing information for that drug.

(a) The NDC assigned to the drug immediately before the drug is received by the registrant for salvaging;

(b) The lot number and expiration date of the salvaged drug product;  and

(c) The name and Unique Facility Identifier for each establishment where the registrant salvages the drug.

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Cite this article: FindLaw.com - Code of Federal Regulations Title 21. Food and Drugs § 21.207.54 What listing information must a registrant submit for a drug that it salvages? - last updated January 02, 2025 | https://codes.findlaw.com/cfr/title-21-food-and-drugs/cfr-sect-21-207-54/

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