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Mycophenolate Mofetil

NDC 0527-5160 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214525
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (200 mg/mL)
Marketing started20210729
Package count1

External sources

Source: openFDA. Public-domain (CC0).