Strength
5 mg/1
Manufacturer
Aurobindo Pharma LimitedNDC
59651013890
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
NEBIVOLOL HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA211053On Market Since
12/17/2021
Pharmacological Classes
Adrenergic beta-Antagonists
beta-Adrenergic Blocker
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