Nebivolol

NDC 33342-459 · Macleods Pharmaceuticals Limited

Generic nameNebivolol

Dosage formTABLET

RouteORAL

Active ingredient(s)NEBIVOLOL HYDROCHLORIDE

Strength10 mg/1

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

Marketing categoryANDA

Packages

33342-459-07 — 30 TABLET in 1 BOTTLE (33342-459-07)

33342-459-10 — 90 TABLET in 1 BOTTLE (33342-459-10)

33342-459-25 — 12 BLISTER PACK in 1 CARTON (33342-459-25) / 10 TABLET in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

29300-375 — Nebivolol Hydrochloride, 29300-376 — Nebivolol Hydrochloride, 29300-377 — Nebivolol Hydrochloride, 29300-378 — Nebivolol Hydrochloride, 31722-585 — Nebivolol, 31722-586 — Nebivolol, 31722-587 — Nebivolol, 31722-588 — Nebivolol, 33342-457 — Nebivolol, 33342-458 — Nebivolol, 33342-460 — Nebivolol, 42291-871 — nebivolol hydrochloride, 42291-872 — nebivolol hydrochloride, 42291-873 — nebivolol hydrochloride, 42291-874 — nebivolol hydrochloride, 50090-5708 — Nebivolol, 50090-5752 — Nebivolol, 50090-5761 — Nebivolol, 50090-7853 — NEBIVOLOL, 51407-483 — 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.