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 opposed to in accordance using this segment. A registrant who performs only salvaging with respect to a drug need to present https://emilioqujad.dsiblogger.com/59653265/the-proleviate-includes-fda-approved-ingredients-diaries