Nebivolol
- Product NDC
- 72189-592
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA212682
- Marketing category
- ANDA
- Substance
- NEBIVOLOL
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 72189-592-60 | 60 TABLET in 1 BOTTLE (72189-592-60) | 2024-10-30 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Nebivolol | Direct_Rx | 2024-10-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |