Tadalafil

NDC 46708-178 · Alembic Pharmaceuticals Limited

Generic nametadalafil

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)TADALAFIL

Strength5 mg/1

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

Marketing categoryANDA

Packages

46708-178-15 — 30 TABLET, COATED in 1 CARTON (46708-178-15)

46708-178-30 — 30 TABLET, COATED in 1 BOTTLE (46708-178-30)

46708-178-71 — 500 TABLET, COATED in 1 BOTTLE (46708-178-71)

46708-178-91 — 1000 TABLET, COATED in 1 BOTTLE (46708-178-91)

FDA lists these products with the same active ingredient.

43547-050 — tadalafil, 43547-051 — tadalafil, 43547-990 — tadalafil, 43598-573 — Tadalafil, 43598-574 — Tadalafil, 43598-575 — Tadalafil, 43598-576 — Tadalafil, 43598-578 — Tadalafil, 46287-045 — Tadalafil, 46708-177 — tadalafil, 46708-179 — tadalafil, 46708-180 — tadalafil, 47335-009 — Tadalafil, 47335-010 — Tadalafil, 47335-011 — Tadalafil, 47335-012 — Tadalafil, 50090-4660 — Tadalafil, 50090-5641 — Tadalafil, 50090-6945 — Tadalafil, 50090-7152 — 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.