Tadalafil

NDC 71335-1620 · Bryant Ranch Prepack

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

71335-1620-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-1620-1)

71335-1620-2 — 10 TABLET, FILM COATED in 1 BOTTLE (71335-1620-2)

71335-1620-3 — 60 TABLET, FILM COATED in 1 BOTTLE (71335-1620-3)

71335-1620-4 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-1620-4)

71335-1620-5 — 20 TABLET, FILM COATED in 1 BOTTLE (71335-1620-5)

71335-1620-6 — 6 TABLET, FILM COATED in 1 BOTTLE (71335-1620-6)

FDA lists these products with the same active ingredient.

71205-269 — 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, 71335-1670 — Tadalafil, 71335-1823 — Tadalafil, 71335-1884 — Tadalafil, 71335-2363 — tadalafil, 71335-2467 — tadalafil, 71335-2583 — tadalafil, 71335-2626 — tadalafil, 71610-461 — Tadalafil, 71610-567 — Tadalafil, 71610-581 — 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.