A registrant who also relabels or repacks a drug that it salvages ought to list the drug it relabels or repacks in accordance with § 207.53 rather than in accordance using this segment. A registrant who performs only salvaging with respect to the drug ought to deliver the following https://edwardz691sso4.bloggadores.com/26392820/the-definitive-guide-to-proleviate-includes-fda-approved-ingredients