NEBIVOLOL

NDC 70518-4648 · REMEDYREPACK INC.

Generic nameNEBIVOLOL

Dosage formTABLET

RouteORAL

Active ingredient(s)NEBIVOLOL HYDROCHLORIDE

Strength5 mg/1

Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Marketing categoryANDA

Packages

70518-4648-0 — 50 POUCH in 1 BOX (70518-4648-0) / 1 TABLET in 1 POUCH (70518-4648-1)

FDA lists these products with the same active ingredient.

63629-9424 — Nebivolol, 67877-390 — Nebivolol, 67877-391 — Nebivolol, 67877-392 — Nebivolol, 67877-393 — Nebivolol, 68462-615 — nebivolol hydrochloride, 68462-616 — nebivolol hydrochloride, 68462-617 — nebivolol hydrochloride, 68462-618 — nebivolol hydrochloride, 70518-3527 — Nebivolol, 70756-025 — Nebivolol, 70756-291 — Nebivolol, 70756-292 — Nebivolol, 70756-293 — Nebivolol, 71209-058 — Nebivolol, 71209-059 — Nebivolol, 71209-060 — Nebivolol, 71209-061 — Nebivolol, 71335-2646 — Nebivolol, 71335-2648 — NEBIVOLOL, +62 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.