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Nebivolol

NDC 62559-277 · ANI Pharmaceuticals, Inc.

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

62559-277-05 — 500 TABLET in 1 BOTTLE (62559-277-05)

62559-277-30 — 30 TABLET in 1 BOTTLE (62559-277-30)

62559-277-90 — 90 TABLET in 1 BOTTLE (62559-277-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-485 — Nebivolol, 51407-486 — Nebivolol, 59651-137 — Nebivolol, 59651-138 — Nebivolol, 59651-139 — Nebivolol, 59651-140 — Nebivolol, 60687-641 — Nebivolol, 60687-652 — Nebivolol, 62559-275 — Nebivolol, 62559-276 — Nebivolol, 62559-278 — Nebivolol, 63629-4693 — Nebivolol, 63629-9423 — Nebivolol, 63629-9424 — Nebivolol, 67877-390 — Nebivolol, 67877-391 — Nebivolol, 67877-392 — Nebivolol, 67877-393 — Nebivolol, 68462-615 — nebivolol hydrochloride, 68462-616 — 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.