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Nebivolol

NDC 72603-871 · NorthStar RxLLC

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

72603-871-01 — 30 TABLET in 1 BOTTLE (72603-871-01)

72603-871-02 — 90 TABLET in 1 BOTTLE (72603-871-02)

Related Codes

Same active ingredient

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, 72241-032 — Nebivolol, 72241-033 — Nebivolol, 72241-034 — Nebivolol, 72241-035 — Nebivolol, 72603-870 — 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.