Nebivolol
NDC 59651-138 · Aurobindo Pharma Limited
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
59651-138-30 — 30 TABLET in 1 BOTTLE (59651-138-30)
59651-138-90 — 90 TABLET in 1 BOTTLE (59651-138-90)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
42291-874 — nebivolol hydrochloride, 50090-5708 — Nebivolol, 50090-5752 — Nebivolol, 50090-5761 — Nebivolol, 50090-7853 — NEBIVOLOL, 51407-483 — Nebivolol, 51407-484 — Nebivolol, 51407-485 — Nebivolol, 51407-486 — Nebivolol, 59651-137 — Nebivolol, 59651-139 — Nebivolol, 59651-140 — Nebivolol, 60687-641 — Nebivolol, 60687-652 — Nebivolol, 62559-275 — Nebivolol, 62559-276 — Nebivolol, 62559-277 — Nebivolol, 62559-278 — Nebivolol, 63629-4693 — Nebivolol, 63629-9423 — Nebivolol, +62 more