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 then in accordance using this segment. A registrant who performs only salvaging with regard to some drug should give the next listing https://jaredweefh.weblogco.com/26952252/proleviate-includes-fda-approved-ingredients-for-dummies