Nadolol 59651-0589
Product NDC
59651-0589- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 7, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA201893
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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 (59651-589-01)