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Leflunomide

NDC 46708-437 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA091369
Dosage form / routeTABLET · ORAL
Active ingredientsLEFLUNOMIDE (20 mg/1)
Marketing started20161201
Package count4

External sources

Source: openFDA. Public-domain (CC0).