Tadalafil

NDC 65862-852 · Aurobindo Pharma Limited

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

65862-852-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65862-852-05)

65862-852-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-852-30)

65862-852-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (65862-852-99)

FDA lists these products with the same active ingredient.

60290-030 — Tadalafil, 62332-177 — tadalafil, 62332-178 — tadalafil, 62332-179 — tadalafil, 62332-180 — tadalafil, 63629-8157 — Tadalafil, 63629-8288 — Tadalafil, 63629-8409 — Tadalafil, 65862-850 — Tadalafil, 65862-851 — Tadalafil, 65862-853 — Tadalafil, 65862-880 — Tadalafil, 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, +230 more

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