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Leflunomide

NDC 59651-349 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA213652
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLEFLUNOMIDE (20 mg/1)
Marketing started20210329
Package count1

External sources

Source: openFDA. Public-domain (CC0).