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Nebivolol

NDC 50090-5708 · A-S Medication Solutions

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

50090-5708-0 — 5 TABLET in 1 BOTTLE (50090-5708-0)

50090-5708-1 — 90 TABLET in 1 BOTTLE (50090-5708-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-587 — Nebivolol, 31722-588 — Nebivolol, 33342-457 — Nebivolol, 33342-458 — Nebivolol, 33342-459 — Nebivolol, 33342-460 — Nebivolol, 42291-871 — nebivolol hydrochloride, 42291-872 — nebivolol hydrochloride, 42291-873 — nebivolol hydrochloride, 42291-874 — nebivolol hydrochloride, 50090-5752 — Nebivolol, 50090-5761 — Nebivolol, 50090-7853 — NEBIVOLOL, 51407-483 — Nebivolol, 51407-484 — Nebivolol, 51407-485 — Nebivolol, 51407-486 — Nebivolol, 59651-137 — Nebivolol, 59651-138 — Nebivolol, 59651-139 — 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.