Nebivolol

NDC 60687-652 · American Health Packaging

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

60687-652-21 — 30 BLISTER PACK in 1 CARTON (60687-652-21) / 1 TABLET in 1 BLISTER PACK (60687-652-11)

FDA lists these products with the same active ingredient.

50090-7853 — NEBIVOLOL, 51407-483 — Nebivolol, 51407-484 — Nebivolol, 51407-485 — Nebivolol, 51407-486 — Nebivolol, 59651-137 — Nebivolol, 59651-138 — Nebivolol, 59651-139 — Nebivolol, 59651-140 — Nebivolol, 60687-641 — Nebivolol, 62559-275 — Nebivolol, 62559-276 — Nebivolol, 62559-277 — Nebivolol, 62559-278 — Nebivolol, 63629-4693 — Nebivolol, 63629-9423 — Nebivolol, 63629-9424 — Nebivolol, 67877-390 — Nebivolol, 67877-391 — Nebivolol, 67877-392 — 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.