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TERIFLUNOMIDE

NDC 68254-5010 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCONCORD BIOTECH LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA218663
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTERIFLUNOMIDE (14 mg/141)
Marketing started20250707
Package count1

External sources

Source: openFDA. Public-domain (CC0).