Tadalafil

NDC 60219-1349 · Amneal Pharmaceuticals NY LLC

Generic nameTadalafil

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)TADALAFIL

Strength20 mg/1

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

Marketing categoryANDA

Packages

60219-1349-3 — 30 TABLET, FILM COATED in 1 BOTTLE (60219-1349-3)

FDA lists these products with the same active ingredient.

50090-7314 — Tadalafil, 50090-7315 — Tadalafil, 50090-7390 — Tadalafil, 50090-7391 — Tadalafil, 51655-063 — Tadalafil, 51655-473 — Tadalafil, 51655-487 — Tadalafil, 60219-1346 — Tadalafil, 60219-1347 — Tadalafil, 60219-1348 — Tadalafil, 60290-027 — Tadalafil, 60290-028 — Tadalafil, 60290-029 — Tadalafil, 60290-030 — Tadalafil, 62332-177 — tadalafil, 62332-178 — tadalafil, 62332-179 — tadalafil, 62332-180 — tadalafil, 63629-8157 — Tadalafil, 63629-8288 — 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.