Nebivolol

NDC 72241-032 · Modavar Pharmaceuticals LLC

Generic nameNebivolol

Dosage formTABLET

RouteORAL

Active ingredient(s)NEBIVOLOL HYDROCHLORIDE

Strength2.5 mg/1

Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Marketing categoryANDA

Packages

72241-032-04 — 90 TABLET in 1 BOTTLE (72241-032-04)

72241-032-05 — 100 TABLET in 1 BOTTLE (72241-032-05)

72241-032-11 — 1000 TABLET in 1 BOTTLE (72241-032-11)

72241-032-22 — 30 TABLET in 1 BOTTLE (72241-032-22)

FDA lists these products with the same active ingredient.

71209-061 — Nebivolol, 71335-2646 — Nebivolol, 71335-2648 — NEBIVOLOL, 71335-3102 — NEBIVOLOL, 72162-2414 — Nebivolol, 72162-2415 — Nebivolol, 72162-2416 — Nebivolol, 72162-2417 — Nebivolol, 72205-150 — NEBIVOLOL, 72205-151 — NEBIVOLOL, 72205-152 — NEBIVOLOL, 72205-153 — NEBIVOLOL, 72241-033 — Nebivolol, 72241-034 — Nebivolol, 72241-035 — Nebivolol, 72603-870 — Nebivolol, 72603-871 — Nebivolol, 72603-872 — Nebivolol, 72603-873 — Nebivolol, 82804-120 — Nebivolol, +62 more

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