Tadalafil

NDC 68071-2554 · NuCare Pharmaceuticals,Inc.

Generic nameTadalafil

Dosage formTABLET

RouteORAL

Active ingredient(s)TADALAFIL

Strength10 mg/1

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

Marketing categoryANDA

Packages

68071-2554-5 — 15 TABLET in 1 BOTTLE (68071-2554-5)

68071-2554-6 — 60 TABLET in 1 BOTTLE (68071-2554-6)

68071-2554-9 — 90 TABLET in 1 BOTTLE (68071-2554-9)

FDA lists these products with the same active ingredient.

66215-812 — macitentan and tadalafil, 66215-814 — macitentan and tadalafil, 66302-467 — Tadalafil, 67184-0523 — Tadalafil, 67184-0524 — Tadalafil, 67184-0525 — Tadalafil, 67184-0526 — Tadalafil, 67296-2237 — tadalafil, 68071-2421 — Tadalafil, 68071-2553 — Tadalafil, 68071-2632 — Tadalafil, 68071-3540 — Tadalafil, 68071-3545 — tadalafil, 68071-3586 — tadalafil, 68071-3598 — tadalafil, 68071-3601 — tadalafil, 68071-3753 — tadalafil, 68071-3758 — tadalafil, 68071-3777 — tadalafil, 68071-3781 — 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.