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Tofacitinib

NDC 42799-970 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA218668
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsTOFACITINIB CITRATE (11 mg/1)
Marketing started20260603
Package count1

External sources

Source: openFDA. Public-domain (CC0).