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mycophenolate mofetil

NDC 72485-415 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerARMAS PHARMACEUTICALS INC
Marketing categoryAbbreviated NDA (generic) · App ANDA216390
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsMYCOPHENOLATE MOFETIL (500 mg/20mL)
Marketing started20230706
Package count1

External sources

Source: openFDA. Public-domain (CC0).