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.