tadalafil

NDC 35573-462 · Burel Pharmaceuticals, LLC

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

35573-462-30 — 30 TABLET, FILM COATED in 1 BOTTLE (35573-462-30)

FDA lists these products with the same active ingredient.

33342-266 — Tadalafil, 33342-267 — Tadalafil, 33342-268 — Tadalafil, 33342-278 — Tadalafil, 35561-254 — Tadalafil, 35561-255 — Tadalafil, 35561-256 — Tadalafil, 35561-257 — Tadalafil, 35573-460 — Tadalafil, 35573-461 — Tadalafil, 35573-463 — Tadalafil, 42291-864 — Tadalafil, 42291-865 — Tadalafil, 42291-866 — Tadalafil, 42291-867 — Tadalafil, 43547-030 — tadalafil, 43547-031 — tadalafil, 43547-032 — tadalafil, 43547-033 — tadalafil, 43547-047 — 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.