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Teriflunomide

NDC 31722-247 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209598
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTERIFLUNOMIDE (14 mg/1)
Marketing started20230313
Package count1

External sources

Source: openFDA. Public-domain (CC0).