A registrant who also relabels or repacks a drug that it salvages must record the drug it relabels or repacks in accordance with § 207.53 as an alternative to in accordance using this part. A registrant who performs only salvaging with regard to the drug must present the next https://canconolidinehelpwithment11987.blogadvize.com/33284719/top-guidelines-of-proleviate-includes-fda-approved-ingredients