Nebivolol 59651-0137
Product NDC
59651-0137- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 17, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA211053
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nebivolol Hydrochloride | 2.5 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
30 TABLET in 1 BOTTLE (59651-137-30)
90 TABLET in 1 BOTTLE (59651-137-90)