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Tofacitinib

NDC 60505-6263 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nametofacitinib
Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA218096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOFACITINIB (5 mg/1)
Marketing started20260603
Package count2

External sources

Source: openFDA. Public-domain (CC0).