Nebivolol
- Product NDC
- 72162-2417
- 11-digit product format
- 721622417
- Labeler code
- 72162
- Product ID
- 72162-2417_754148cb-fd38-42b8-9434-05a45c1bd89b
- 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
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nebivolol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NEBIVOLOL HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JGS34J7L9I |
| Rxcui | 387013 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2417-3 | Nebivolol | 30 in 1 BOTTLE | TABLET | 30 | | 100 |
| 72162-2417-9 | Nebivolol | 90 in 1 BOTTLE | TABLET | 90 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2417 | NEBIVOLOL TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20241102_9a5e1bd8-f2b6-42e6-972d-09418528cd63.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2417-3 | 72162241703 | 30 TABLET in 1 BOTTLE (72162-2417-3) | 30 tablet | 2024-10-31 | No | No | Current |
| 72162-2417-9 | 72162241709 | 90 TABLET in 1 BOTTLE (72162-2417-9) | 90 tablet | 2024-10-31 | No | No | Current |