FDA NDC Directory · JSON-LD · Markdown

TOFACITINIB

NDC 42571-268 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nametofacitinib
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA209738
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOFACITINIB CITRATE (5 mg/1)
Marketing started20260603
Package count4

External sources

Source: openFDA. Public-domain (CC0).