Nebivolol
- Product NDC
- 72162-2415
- 11-digit product format
- 721622415
- Labeler code
- 72162
- Product ID
- 72162-2415_2124870a-c883-46ee-8f1d-bcb1c01ef301
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208717
- Marketing category
- ANDA
- Marketing start
- 2017-12-29
- Substance
- NEBIVOLOL HYDROCHLORIDE
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| JGS34J7L9I | NEBIVOLOL HYDROCHLORIDE | 152520-56-4 | NEBIVOLOL HYDROCHLORIDE |
| 030Y90569U | NEBIVOLOL | 118457-14-0 | Nebivolol |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2415-3 | 72162241503 | 30 TABLET in 1 BOTTLE (72162-2415-3) | 30 tablet | 2024-10-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Nebivolol | Bryant Ranch Prepack | 2024-10-31 | HUMAN PRESCRIPTION DRUG LABEL | 101 |