FDA NDC Directory · JSON-LD · Markdown

tofacitinib

NDC 70710-1589 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209829
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOFACITINIB CITRATE (10 mg/1)
Marketing started20260605
Package count3

External sources

Source: openFDA. Public-domain (CC0).