NDC 31722-588 – Nebivolol
Nebivolol Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC31722-588
Product details
- Brand name
- Nebivolol
- Generic name
- Nebivolol
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203825
- Marketed since
- September 17, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Nebivolol Hydrochloride 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 31722-588-01 | 100 TABLET in 1 BOTTLE (31722-588-01) | Sep 17, 2021 |
| 31722-588-30 | 30 TABLET in 1 BOTTLE (31722-588-30) | Sep 17, 2021 |
| 31722-588-32 | 10 BLISTER PACK in 1 CARTON (31722-588-32) / 10 TABLET in 1 BLISTER PACK (31722-588-31) | Sep 17, 2021 |
| 31722-588-34 | 18 BLISTER PACK in 1 CARTON (31722-588-34) / 7 TABLET in 1 BLISTER PACK (31722-588-33) | Sep 17, 2021 |
| 31722-588-90 | 90 TABLET in 1 BOTTLE (31722-588-90) | Sep 17, 2021 |
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