FDA NDC Directory · JSON-LD · Markdown

TOFACITINIB

NDC 70069-842 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA220137
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOFACITINIB CITRATE (10 mg/1)
Marketing started20260603
Package count1

External sources

Source: openFDA. Public-domain (CC0).