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nebivolol

NDC 68462-617 · Glenmark Pharmaceuticals Inc., USA

Generic namenebivolol hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)NEBIVOLOL HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

68462-617-01 — 100 TABLET in 1 BOTTLE (68462-617-01)

68462-617-11 — 10 BLISTER PACK in 1 CARTON (68462-617-11) / 10 TABLET in 1 BLISTER PACK

68462-617-30 — 30 TABLET in 1 BOTTLE (68462-617-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68462-618 — nebivolol hydrochloride, 70518-3527 — Nebivolol, 70518-4648 — NEBIVOLOL, 70756-025 — Nebivolol, 70756-291 — Nebivolol, 70756-292 — Nebivolol, 70756-293 — Nebivolol, 71209-058 — Nebivolol, 71209-059 — Nebivolol, 71209-060 — 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.