tadalafil

NDC 29300-286 · Unichem Pharmaceuticals (USA), Inc.

Generic nametadalafil

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)TADALAFIL

Strength2.5 mg/1

Pharmacologic classPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

Marketing categoryANDA

Packages

29300-286-01 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-286-01)

29300-286-05 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-286-05)

29300-286-13 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-286-13)

29300-286-82 — 2 BLISTER PACK in 1 CARTON (29300-286-82) / 15 TABLET, FILM COATED in 1 BLISTER PACK (29300-286-51)

FDA lists these products with the same active ingredient.

16729-372 — Tadalafil, 24979-727 — Tadalafil, 24979-728 — Tadalafil, 24979-729 — Tadalafil, 24979-730 — Tadalafil, 27241-111 — Tadalafil, 27241-112 — Tadalafil, 27241-113 — Tadalafil, 27241-114 — Tadalafil, 27241-123 — Tadalafil, 29300-287 — tadalafil, 29300-288 — tadalafil, 29300-289 — tadalafil, 31722-643 — Tadalafil, 31722-644 — Tadalafil, 31722-645 — Tadalafil, 31722-646 — Tadalafil, 31722-647 — Tadalafil, 33342-265 — Tadalafil, 33342-266 — Tadalafil, +230 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.