A registrant who also relabels or repacks a drug that it salvages should list the drug it relabels or repacks in accordance with § 207.53 rather then in accordance with this area. A registrant who performs only salvaging with respect to the drug must supply the following listing facts https://codyntume.ka-blogs.com/80123233/proleviate-includes-fda-approved-ingredients-things-to-know-before-you-buy