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nebivolol

NDC 24689-159 · Apnar Pharma LP

Generic namenebivolol hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)NEBIVOLOL HYDROCHLORIDE
Strength2.5 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

24689-159-01 — 30 TABLET in 1 BOTTLE (24689-159-01)

24689-159-02 — 90 TABLET in 1 BOTTLE (24689-159-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0456-1402 — nebivolol hydrochloride, 0456-1405 — nebivolol hydrochloride, 0456-1410 — nebivolol hydrochloride, 0456-1420 — nebivolol hydrochloride, 24689-160 — nebivolol hydrochloride, 24689-161 — nebivolol hydrochloride, 24689-162 — nebivolol hydrochloride, 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, 33342-459 — Nebivolol, 33342-460 — Nebivolol, 42291-871 — nebivolol hydrochloride, +62 more

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