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 using this type of section. A registrant who performs only salvaging with respect to a drug ought to https://martinwmkdu.newbigblog.com/32681131/proleviate-includes-fda-approved-ingredients-fundamentals-explained