tadalafil

NDC 76420-856 · Asclemed USA, Inc.

Generic nametadalafil

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)TADALAFIL

Strength10 mg/1

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

Marketing categoryANDA

Packages

76420-856-01 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-856-01)

76420-856-05 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-856-05)

76420-856-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-856-30)

76420-856-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-856-60)

76420-856-90 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-856-90)

FDA lists these products with the same active ingredient.

76420-543 — Tadalafil, 76420-544 — Tadalafil, 76420-546 — TADALAFIL, 76420-551 — Tadalafil, 76420-552 — Tadalafil, 76420-553 — Tadalafil, 76420-554 — Tadalafil, 76420-642 — Tadalafil, 76420-854 — tadalafil, 76420-855 — tadalafil, 76420-857 — tadalafil, 80425-0443 — Tadalafil, 82009-077 — Tadalafil, 82009-079 — Tadalafil, 82009-080 — Tadalafil, 82804-040 — Tadalafil, 82804-041 — Tadalafil, 82804-042 — Tadalafil, 82804-112 — tadalafil, 82804-224 — 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.