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Mycophenolate Mofetil

NDC 50268-558 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA091249
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (500 mg/1)
Marketing started20230515
Package count1

External sources

Source: openFDA. Public-domain (CC0).