StacksVerified U.S. regulatory reference

21 CFR §207.54

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
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.
  1. (a)The NDC assigned to the drug immediately before the drug is received by the registrant for salvaging;
  2. (b)The lot number and expiration date of the salvaged drug product; and
  3. (c)The name and Unique Facility Identifier for each establishment where the registrant salvages the drug.