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NEBIVOLOL

NDC 71335-2648 · Bryant Ranch Prepack

Generic nameNEBIVOLOL
Dosage formTABLET
RouteORAL
Active ingredient(s)NEBIVOLOL HYDROCHLORIDE
Strength5 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

71335-2648-1 — 30 TABLET in 1 BOTTLE (71335-2648-1)

71335-2648-2 — 90 TABLET in 1 BOTTLE (71335-2648-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4648 — NEBIVOLOL, 70756-025 — Nebivolol, 70756-291 — Nebivolol, 70756-292 — Nebivolol, 70756-293 — Nebivolol, 71209-058 — Nebivolol, 71209-059 — Nebivolol, 71209-060 — Nebivolol, 71209-061 — Nebivolol, 71335-2646 — 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, 72241-032 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels