FDA NDC Directory · JSON-LD · Markdown

Tofacitinib

NDC 33342-541 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA219530
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOFACITINIB CITRATE (5 mg/1)
Marketing started20260603
Package count3

External sources

Source: openFDA. Public-domain (CC0).