Strength
20 mg/1
Manufacturer
BluePoint LaboratoriesNDC
68001031700
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
NADOLOLApproval Type
Generic (ANDA)
FDA Application
ANDA203455On Market Since
2/23/2016
Pharmacological Classes
Adrenergic beta-Antagonists
beta-Adrenergic Blocker
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