tadalafil

NDC 71821-007 · VKT Pharma 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

71821-007-01 — 15 CARTON in 1 BLISTER PACK (71821-007-01) / 30 TABLET, FILM COATED in 1 CARTON

71821-007-02 — 30 TABLET, FILM COATED in 1 BOTTLE (71821-007-02)

FDA lists these products with the same active ingredient.

71610-461 — Tadalafil, 71610-567 — Tadalafil, 71610-581 — Tadalafil, 71610-603 — Tadalafil, 71610-728 — Tadalafil, 71610-896 — Tadalafil, 71610-903 — tadalafil, 71610-908 — tadalafil, 71610-909 — tadalafil, 71821-006 — Tadalafil, 71821-008 — Tadalafil, 71821-009 — Tadalafil, 72189-145 — TADALAFIL, 72303-0822 — Tadalafil, 72303-0823 — Tadalafil, 72303-0824 — Tadalafil, 72303-0825 — Tadalafil, 72603-781 — Tadalafil, 72603-782 — Tadalafil, 72603-783 — 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.