Nebivolol
NDC 70756-292 · Lifestar Pharma LLC
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
70756-292-30 — 30 TABLET in 1 BOTTLE (70756-292-30)
70756-292-90 — 90 TABLET in 1 BOTTLE (70756-292-90)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
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, 70518-4648 — NEBIVOLOL, 70756-025 — Nebivolol, 70756-291 — Nebivolol, 70756-293 — Nebivolol, 71209-058 — Nebivolol, 71209-059 — Nebivolol, 71209-060 — Nebivolol, 71209-061 — Nebivolol, 71335-2646 — Nebivolol, 71335-2648 — NEBIVOLOL, 71335-3102 — NEBIVOLOL, 72162-2414 — Nebivolol, 72162-2415 — Nebivolol, +62 more