tadalafil

NDC 71335-2583 · Bryant Ranch Prepack

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

71335-2583-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2583-1)

71335-2583-2 10 TABLET, FILM COATED in 1 BOTTLE (71335-2583-2)

71335-2583-3 90 TABLET, FILM COATED in 1 BOTTLE (71335-2583-3)

71335-2583-4 5 TABLET, FILM COATED in 1 BOTTLE (71335-2583-4)

71335-2583-5 60 TABLET, FILM COATED in 1 BOTTLE (71335-2583-5)

71335-2583-6 20 TABLET, FILM COATED in 1 BOTTLE (71335-2583-6)

71335-2583-7 15 TABLET, FILM COATED in 1 BOTTLE (71335-2583-7)

71335-2583-8 100 TABLET, FILM COATED in 1 BOTTLE (71335-2583-8)

FDA lists these products with the same active ingredient.

71205-754 — tadalafil, 71335-1255 — Tadalafil, 71335-1491 — Tadalafil, 71335-1587 — Tadalafil, 71335-1620 — Tadalafil, 71335-1670 — Tadalafil, 71335-1823 — Tadalafil, 71335-1884 — Tadalafil, 71335-2363 — tadalafil, 71335-2467 — tadalafil, 71335-2626 — tadalafil, 71610-461 — Tadalafil, 71610-567 — Tadalafil, 71610-581 — Tadalafil, 71610-603 — Tadalafil, 71610-728 — Tadalafil, 71610-896 — Tadalafil, 71610-903 — tadalafil, 71610-908 — tadalafil, 71610-909 — 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.