Tadalafil

NDC 60290-030 · Umedica Laboratories USA Inc.

Generic nameTadalafil

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)TADALAFIL

Strength20 mg/1

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

Marketing categoryANDA

Packages

60290-030-01 — 30 TABLET, FILM COATED in 1 BOTTLE (60290-030-01)

60290-030-02 — 1000 TABLET, FILM COATED in 1 BOTTLE (60290-030-02)

60290-030-03 — 30 TABLET, FILM COATED in 1 BLISTER PACK (60290-030-03)

60290-030-04 — 500 TABLET, FILM COATED in 1 BOTTLE (60290-030-04)

60290-030-05 — 5000 TABLET, FILM COATED in 1 BOTTLE (60290-030-05)

FDA lists these products with the same active ingredient.

51655-063 — Tadalafil, 51655-473 — Tadalafil, 51655-487 — Tadalafil, 60219-1346 — Tadalafil, 60219-1347 — Tadalafil, 60219-1348 — Tadalafil, 60219-1349 — Tadalafil, 60290-027 — Tadalafil, 60290-028 — Tadalafil, 60290-029 — 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, 65862-852 — 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.