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tofacitinib

NDC 70710-1243 · Zydus Pharmaceuticals USA Inc.

Generic nametofacitinib
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)TOFACITINIB CITRATE
Strength5 mg/1
Pharmacologic classJanus Kinase Inhibitor [EPC], Janus Kinase Inhibitors [MoA]
Marketing categoryANDA

Packages

70710-1243-6 — 60 TABLET, FILM COATED in 1 BOTTLE (70710-1243-6)

70710-1243-8 — 180 TABLET, FILM COATED in 1 BOTTLE (70710-1243-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60505-4858 — tofacitinib, 63539-012 — tofacitinib, 63539-016 — tofacitinib, 63539-029 — tofacitinib, 63539-501 — tofacitinib, 63539-502 — tofacitinib, 70069-841 — TOFACITINIB, 70069-842 — TOFACITINIB, 70095-008 — Tofacitinib, 70377-057 — Tofacitinib, 70710-1353 — tofacitinib, 70710-1589 — tofacitinib, 70710-1727 — tofacitinib, 70771-1627 — tofacitinib, 70771-1628 — tofacitinib, 70771-1821 — tofacitinib, 70771-1967 — tofacitinib, 71085-099 — Tofacitinib, 72205-121 — TOFACITINIB, 72205-139 — Tofacitinib, +27 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.