A registrant who also relabels or repacks a drug that it salvages need to list the drug it relabels or repacks in accordance with § 207.fifty three as an alternative to in accordance with this segment. A registrant who performs only salvaging with respect to a drug need to https://kinga950qhx6.blogdiloz.com/26288453/the-proleviate-includes-fda-approved-ingredients-diaries