A registrant who also relabels or repacks a drug that it salvages should checklist the drug it relabels or repacks in accordance with § 207.53 as an alternative to in accordance with this segment. A registrant who performs only salvaging with respect to a drug need to present the https://marconkcri.bloggosite.com/33108882/proleviate-includes-fda-approved-ingredients-for-dummies