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TOFACITINIB CITRATE

NDC 85972-121 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerStellon Biotech Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218821
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOFACITINIB CITRATE (8.08 mg/1)
Marketing started20261001
Package count1

External sources

Source: openFDA. Public-domain (CC0).