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Mycophenolate mofetil

NDC 64380-725 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090456
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (500 mg/1)
Marketing started20101106
Package count2

External sources

Source: openFDA. Public-domain (CC0).