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Mycophenolate mofetil

NDC 0904-7078 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA090456
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (500 mg/1)
Marketing started20101106
Package count1

External sources

Source: openFDA. Public-domain (CC0).