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teriflunomide

NDC 68462-424 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA209663
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTERIFLUNOMIDE (14 mg/1)
Marketing started20230119
Package count3

External sources

Source: openFDA. Public-domain (CC0).