Tadalafil

NDC 43598-573 · Dr.Reddys Laboratories 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

43598-573-30 — 30 TABLET, FILM COATED in 1 BOTTLE (43598-573-30)

43598-573-31 — 3 BLISTER PACK in 1 CARTON (43598-573-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-573-79)

43598-573-60 — 60 TABLET, FILM COATED in 1 BOTTLE (43598-573-60)

FDA lists these products with the same active ingredient.

42291-867 — Tadalafil, 43547-030 — tadalafil, 43547-031 — tadalafil, 43547-032 — tadalafil, 43547-033 — tadalafil, 43547-047 — tadalafil, 43547-049 — tadalafil, 43547-050 — tadalafil, 43547-051 — tadalafil, 43547-990 — tadalafil, 43598-574 — Tadalafil, 43598-575 — Tadalafil, 43598-576 — Tadalafil, 43598-578 — Tadalafil, 46287-045 — Tadalafil, 46708-177 — tadalafil, 46708-178 — tadalafil, 46708-179 — tadalafil, 46708-180 — tadalafil, 47335-009 — 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.