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Teriflunomide

NDC 69539-033 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMSN LABORATORIES PRIVATE LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA209623
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTERIFLUNOMIDE (14 mg/1)
Marketing started20190424
Package count1

External sources

Source: openFDA. Public-domain (CC0).