Tadalafil

NDC 72865-104 · XLCare Pharmaceuticals 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

72865-104-30 — 30 TABLET, FILM COATED in 1 BOTTLE (72865-104-30)

FDA lists these products with the same active ingredient.

72603-782 — Tadalafil, 72603-783 — Tadalafil, 72603-784 — Tadalafil, 72789-184 — Tadalafil, 72789-324 — Tadalafil, 72789-344 — Tadalafil, 72789-396 — Tadalafil, 72789-407 — Tadalafil, 72789-408 — Tadalafil, 72789-430 — Tadalafil, 72865-106 — Tadalafil, 72865-107 — Tadalafil, 72865-108 — Tadalafil, 73190-032 — tadalafil, 75834-247 — Tadalafil, 75834-248 — Tadalafil, 75834-249 — Tadalafil, 75834-250 — Tadalafil, 76420-126 — Tadalafil, 76420-541 — 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.