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tofacitinib

NDC 70710-1353 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214264
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsTOFACITINIB CITRATE (11 mg/1)
Marketing started20260520
Package count2

External sources

Source: openFDA. Public-domain (CC0).