Tadalafil

NDC 70771-1478 · Zydus Lifesciences Limited

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

70771-1478-0 — 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1478-0)

70771-1478-1 — 100 TABLET, FILM COATED in 1 BOTTLE (70771-1478-1)

70771-1478-3 — 30 TABLET, FILM COATED in 1 BOTTLE (70771-1478-3)

70771-1478-4 — 2 BLISTER PACK in 1 CARTON (70771-1478-4) / 15 TABLET, FILM COATED in 1 BLISTER PACK

70771-1478-5 — 500 TABLET, FILM COATED in 1 BOTTLE (70771-1478-5)

70771-1478-9 — 90 TABLET, FILM COATED in 1 BOTTLE (70771-1478-9)

FDA lists these products with the same active ingredient.

69238-1349 — Tadalafil, 70518-3434 — Tadalafil, 70518-3864 — tadalafil, 70518-3931 — tadalafil, 70518-4534 — Tadalafil, 70518-4549 — Tadalafil, 70518-4605 — TADALAFIL, 70771-1475 — Tadalafil, 70771-1476 — Tadalafil, 70771-1477 — Tadalafil, 70954-433 — Tadalafil, 70954-434 — Tadalafil, 70954-435 — Tadalafil, 71205-268 — Tadalafil, 71205-269 — Tadalafil, 71205-502 — Tadalafil, 71205-720 — Tadalafil, 71205-734 — Tadalafil, 71205-735 — Tadalafil, 71205-736 — 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.