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Mycophenolate Mofetil

NDC 0054-0163 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065410
Dosage form / routeCAPSULE · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (250 mg/1)
Marketing started20080729
Package count2

External sources

Source: openFDA. Public-domain (CC0).