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 in lieu of in accordance with this portion. A registrant who performs only salvaging with respect to your drug need to deliver the https://trentonrnevl.smblogsites.com/26919708/not-known-facts-about-proleviate-includes-fda-approved-ingredients