Tadalafil

NDC 82968-002 · FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED

Generic nameTadalafil

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)TADALAFIL

Strength5 mg/1

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

Marketing categoryANDA

Packages

82968-002-01 — 30 TABLET, FILM COATED in 1 BOTTLE (82968-002-01)

82968-002-02 — 2 BLISTER PACK in 1 CARTON (82968-002-02) / 15 TABLET, FILM COATED in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

76420-553 — Tadalafil, 76420-554 — Tadalafil, 76420-642 — Tadalafil, 76420-854 — tadalafil, 76420-855 — tadalafil, 76420-856 — 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, 82868-028 — Tadalafil, 82968-001 — Tadalafil, 82968-003 — Tadalafil, 82968-005 — 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.