Nebivolol
- Product NDC
- 82804-120
- 11-digit product format
- 828040120
- Labeler code
- 82804
- Product ID
- 82804-120_c6606db5-3937-4e90-9870-3cbfa4ec909e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203825
- Marketing category
- ANDA
- Marketing start
- 2021-09-17
- Substance
- NEBIVOLOL HYDROCHLORIDE
- Active strength
- 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 |
|---|
| 82804-120-90 | 82804012090 | 90 TABLET in 1 BOTTLE (82804-120-90) | 90 tablet | 2024-07-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Nebivolol | Proficient Rx LP | 2024-07-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |