A registrant who also relabels or repacks a drug that it salvages must record the drug it relabels or repacks in accordance with § 207.fifty three as an alternative to in accordance using this type of portion. A registrant who performs only salvaging with regard to the drug will https://louisuohwm.izrablog.com/27381490/the-definitive-guide-to-proleviate-includes-fda-approved-ingredients