Tadalafil

NDC 71610-581 · Aphena Pharma Solutions - Tennessee, 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

71610-581-04 — 4 TABLET, FILM COATED in 1 BOTTLE (71610-581-04)

71610-581-06 — 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-581-06)

71610-581-12 — 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-581-12)

71610-581-39 — 1440 TABLET, FILM COATED in 1 BOTTLE (71610-581-39)

71610-581-52 — 18 TABLET, FILM COATED in 1 BOTTLE (71610-581-52)

FDA lists these products with the same active ingredient.

71335-1620 — Tadalafil, 71335-1670 — Tadalafil, 71335-1823 — Tadalafil, 71335-1884 — Tadalafil, 71335-2363 — tadalafil, 71335-2467 — tadalafil, 71335-2583 — tadalafil, 71335-2626 — tadalafil, 71610-461 — Tadalafil, 71610-567 — Tadalafil, 71610-603 — Tadalafil, 71610-728 — Tadalafil, 71610-896 — Tadalafil, 71610-903 — tadalafil, 71610-908 — tadalafil, 71610-909 — tadalafil, 71821-006 — Tadalafil, 71821-007 — Tadalafil, 71821-008 — Tadalafil, 71821-009 — 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.