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 instead of in accordance with this particular segment. A registrant who performs only salvaging with respect to some drug should deliver the next listing https://haynesy162ulz6.shoutmyblog.com/26604049/proleviate-includes-fda-approved-ingredients-things-to-know-before-you-buy