Tadalafil

NDC 68382-896 · Zydus Pharmaceuticals USA Inc.

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

68382-896-01 — 100 TABLET, FILM COATED in 1 BOTTLE (68382-896-01)

68382-896-05 — 500 TABLET, FILM COATED in 1 BOTTLE (68382-896-05)

68382-896-06 — 30 TABLET, FILM COATED in 1 BOTTLE (68382-896-06)

68382-896-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (68382-896-10)

68382-896-16 — 90 TABLET, FILM COATED in 1 BOTTLE (68382-896-16)

68382-896-99 — 2 BLISTER PACK in 1 CARTON (68382-896-99) / 15 TABLET, FILM COATED in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

68071-3753 — tadalafil, 68071-3758 — tadalafil, 68071-3777 — tadalafil, 68071-3781 — tadalafil, 68071-3800 — tadalafil, 68071-3929 — Tadalafil, 68071-3936 — Tadalafil, 68071-5186 — Tadalafil, 68071-5202 — Tadalafil, 68180-914 — Tadalafil, 68382-897 — Tadalafil, 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, +230 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.