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.
The NDC assigned to the drug immediately before the drug is received by the registrant for salvaging;
The lot number and expiration date of the salvaged drug product; and
The name and Unique Facility Identifier for each establishment where the registrant salvages the drug.
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