Nebivolol 67877-0392
Product NDC
67877-0392- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 16, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA203828
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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(4)
100 TABLET in 1 BOTTLE (67877-392-01)
30 TABLET in 1 BOTTLE (67877-392-30)
1 BLISTER PACK in 1 CARTON (67877-392-33) / 10 TABLET in 1 BLISTER PACK
90 TABLET in 1 BOTTLE (67877-392-90)