§ 207.54. What listing information must a registrant submit for a drug that it salvages?
99 words·~1 min read·
/us/cfr/t21/s§ 207.54·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
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.