FDA NDC Directory · JSON-LD · Markdown

XELJANZ

NDC 63539-012 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nametofacitinib
Labeler / ManufacturerU.S. Pharmaceuticals
Marketing categoryNew Drug Application (innovator) · App NDA203214
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOFACITINIB CITRATE (5 mg/1)
Marketing started20121108
Package count1

External sources

Source: openFDA. Public-domain (CC0).