Nebivolol 70518-4648
Product NDC
70518-4648- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 28, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA217397
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nebivolol Hydrochloride | 5 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
50 POUCH in 1 BOX (70518-4648-0) / 1 TABLET in 1 POUCH (70518-4648-1)