FDA NDC Directory · JSON-LD · Markdown

Tofacitinib

NDC 72205-139 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217299
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOFACITINIB CITRATE (5 mg/1)
Marketing started20260603
Package count2

External sources

Source: openFDA. Public-domain (CC0).