Nebivolol 72189-0592
Product NDC
72189-0592- Manufacturer
- Direct_rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 30, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA212682
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nebivolol | 20 mg/1 |
Drug Class
beta-Adrenergic Blocker [EPC]Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
60 TABLET in 1 BOTTLE (72189-592-60)