Nadolol 68001-0317
Product NDC
68001-0317- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 23, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA203455
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nadolol | 20 mg/1 |
Drug Class
beta-Adrenergic Blocker [EPC]Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE (68001-317-00)