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 instead of in accordance with this section. A registrant who performs only salvaging with regard into a drug should provide the subsequent listing https://elliotazwtn.wikidirective.com/6657652/the_single_best_strategy_to_use_for_proleviate_includes_fda_approved_ingredients