A registrant who also relabels or repacks a drug that it salvages should list the drug it relabels or repacks in accordance with § 207.53 in lieu of in accordance with this portion. A registrant who performs only salvaging with regard to the drug should offer the subsequent listing https://tysonwgjka.blogdeazar.com/26977637/proleviate-includes-fda-approved-ingredients-things-to-know-before-you-buy