FDA NDC Directory · JSON-LD · Markdown

Teriflunomide

NDC 70710-1114 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209668
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTERIFLUNOMIDE (7 mg/1)
Marketing started20230214
Package count2

External sources

Source: openFDA. Public-domain (CC0).