FDA NDC Directory · JSON-LD · Markdown

TOFACITINIB

NDC 70095-008 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameTofacitinib
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218407
Dosage form / routeSOLUTION · ORAL
Active ingredientsTOFACITINIB CITRATE (1 mg/mL)
Marketing started20260603
Package count1

External sources

Source: openFDA. Public-domain (CC0).