Nadolol 60687-0302
Product NDC
60687-0302- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 22, 2017
- 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]