NDC 67877-392 – Nebivolol
Nebivolol Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC67877-392
Product details
- Brand name
- Nebivolol
- Generic name
- Nebivolol
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203828
- Marketed since
- September 16, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Nebivolol Hydrochloride 5 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-392-01 | 100 TABLET in 1 BOTTLE (67877-392-01) | Sep 16, 2021 |
| 67877-392-30 | 30 TABLET in 1 BOTTLE (67877-392-30) | Sep 16, 2021 |
| 67877-392-33 | 1 BLISTER PACK in 1 CARTON (67877-392-33) / 10 TABLET in 1 BLISTER PACK | Sep 16, 2021 |
| 67877-392-90 | 90 TABLET in 1 BOTTLE (67877-392-90) | Sep 16, 2021 |
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