Tadalafil

NDC 69238-1346 · Amneal Pharmaceuticals NY LLC

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

69238-1346-3 — 30 TABLET, FILM COATED in 1 BOTTLE (69238-1346-3)

FDA lists these products with the same active ingredient.

68382-898 — Tadalafil, 68382-899 — Tadalafil, 68788-4018 — TADALAFIL, 68788-4083 — tadalafil, 68788-8153 — Tadalafil, 68788-8292 — Tadalafil, 68788-8445 — Tadalafil, 68788-8465 — tadalafil, 68788-8664 — tadalafil, 69097-526 — Tadalafil, 69238-1347 — Tadalafil, 69238-1348 — Tadalafil, 69238-1349 — Tadalafil, 70518-3434 — Tadalafil, 70518-3864 — tadalafil, 70518-3931 — tadalafil, 70518-4534 — Tadalafil, 70518-4549 — Tadalafil, 70518-4605 — TADALAFIL, 70771-1475 — 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.