Tadalafil

NDC 47335-009 · Sun Pharmaceutical Industries, Inc.

Generic nameTadalafil

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)TADALAFIL

Strength2.5 mg/1

Pharmacologic classPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

Marketing categoryANDA

Packages

47335-009-64 — 2 BLISTER PACK in 1 CARTON (47335-009-64) / 15 TABLET, FILM COATED in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

43598-573 — Tadalafil, 43598-574 — Tadalafil, 43598-575 — Tadalafil, 43598-576 — Tadalafil, 43598-578 — Tadalafil, 46287-045 — Tadalafil, 46708-177 — tadalafil, 46708-178 — tadalafil, 46708-179 — tadalafil, 46708-180 — tadalafil, 47335-010 — Tadalafil, 47335-011 — Tadalafil, 47335-012 — Tadalafil, 50090-4660 — Tadalafil, 50090-5641 — Tadalafil, 50090-6945 — Tadalafil, 50090-7152 — tadalafil, 50090-7314 — Tadalafil, 50090-7315 — Tadalafil, 50090-7390 — Tadalafil, +230 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.