A registrant who also relabels or repacks a drug that it salvages should list the drug it relabels or repacks in accordance with § 207.fifty three rather than in accordance using this portion. A registrant who performs only salvaging with respect to a drug ought to offer the next https://tysontjuhf.blogolenta.com/23676212/the-basic-principles-of-proleviate-includes-fda-approved-ingredients