A registrant who also relabels or repacks a drug that it salvages have to list the drug it relabels or repacks in accordance with § 207.53 instead of in accordance using this segment. A registrant who performs only salvaging with respect to a drug have to provide the next https://gunnerqmfzp.blogdiloz.com/26587562/top-guidelines-of-proleviate-includes-fda-approved-ingredients