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Mycophenolic Acid

NDC 60505-2965 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerApotex Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA091558
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsMYCOPHENOLATE SODIUM (180 mg/1)
Marketing started20120821
Package count1

External sources

Source: openFDA. Public-domain (CC0).