Tadalafil

NDC 71205-269 · Proficient Rx LP

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

71205-269-30 — 30 TABLET, FILM COATED in 1 BOTTLE (71205-269-30)

71205-269-60 — 60 TABLET, FILM COATED in 1 BOTTLE (71205-269-60)

71205-269-90 — 90 TABLET, FILM COATED in 1 BOTTLE (71205-269-90)

FDA lists these products with the same active ingredient.

70518-4549 — Tadalafil, 70518-4605 — TADALAFIL, 70771-1475 — Tadalafil, 70771-1476 — Tadalafil, 70771-1477 — Tadalafil, 70771-1478 — Tadalafil, 70954-433 — Tadalafil, 70954-434 — Tadalafil, 70954-435 — Tadalafil, 71205-268 — Tadalafil, 71205-502 — Tadalafil, 71205-720 — Tadalafil, 71205-734 — Tadalafil, 71205-735 — Tadalafil, 71205-736 — Tadalafil, 71205-754 — tadalafil, 71335-1255 — Tadalafil, 71335-1491 — Tadalafil, 71335-1587 — Tadalafil, 71335-1620 — 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.