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leflunomide

NDC 70710-1158 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212308
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLEFLUNOMIDE (20 mg/1)
Marketing started20190426
Package count3

External sources

Source: openFDA. Public-domain (CC0).