A registrant who also relabels or repacks a drug that it salvages should listing the drug it relabels or repacks in accordance with § 207.fifty three rather then in accordance with this segment. A registrant who performs only salvaging with respect to a drug need to supply the following https://isconolidineanopiate71274.blog2learn.com/74767631/new-step-by-step-map-for-proleviate-includes-fda-approved-ingredients