A registrant who also relabels or repacks a drug that it salvages have to listing the drug it relabels or repacks in accordance with § 207.53 in lieu of in accordance using this portion. A registrant who performs only salvaging with regard to the drug must supply the following https://fredw950slb7.blogozz.com/26300137/the-greatest-guide-to-proleviate-includes-fda-approved-ingredients