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Mycophenolate Mofetil

NDC 71610-033 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namemycophenolate mofetil
Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065521
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (500 mg/1)
Marketing started20150106
Package count7

External sources

Source: openFDA. Public-domain (CC0).