A registrant who also relabels or repacks a drug that it salvages will have to checklist the drug it relabels or repacks in accordance with § 207.fifty three as opposed to in accordance with this particular portion. A registrant who performs only salvaging with respect to a drug must https://trentonbxphx.mpeblog.com/49935977/the-definitive-guide-to-proleviate-includes-fda-approved-ingredients