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Teriflunomide

NDC 0378-0628 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209702
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTERIFLUNOMIDE (14 mg/1)
Marketing started20230214
Package count1

External sources

Source: openFDA. Public-domain (CC0).