A registrant who also relabels or repacks a drug that it salvages need to list the drug it relabels or repacks in accordance with § 207.53 in lieu of in accordance with this portion. A registrant who performs only salvaging with respect to a drug ought to supply the https://ricardotdwsj.bluxeblog.com/58875222/the-single-best-strategy-to-use-for-proleviate-includes-fda-approved-ingredients