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Tofacitinib

NDC 72205-140 · Novadoz Pharmaceuticals LLC

Generic nameTofacitinib
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)TOFACITINIB CITRATE
Strength10 mg/1
Pharmacologic classJanus Kinase Inhibitor [EPC], Janus Kinase Inhibitors [MoA]
Marketing categoryANDA

Packages

72205-140-18 — 180 TABLET, FILM COATED in 1 BOTTLE (72205-140-18)

72205-140-28 — 28 TABLET, FILM COATED in 1 BOTTLE (72205-140-28)

72205-140-60 — 60 TABLET, FILM COATED in 1 BOTTLE (72205-140-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70095-008 — Tofacitinib, 70377-057 — Tofacitinib, 70710-1243 — 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, 73190-100 — Tofacitinib, 73190-101 — Tofacitinib, 73190-102 — tofacitinib, 76282-816 — TOFACITINIB, 76333-111 — TOFACITINIB, 77771-567 — Tofacitinib citrate, 84677-048 — 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.