Nebivolol
- Product NDC
- 51407-483
- 11-digit product format
- 514070483
- Labeler code
- 51407
- Product ID
- 51407-483_48392f96-85ae-e631-e063-6294a90a2568
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA203659
- Marketing category
- ANDA
- Marketing start
- 2015-04-16
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nebivolol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NEBIVOLOL HYDROCHLORIDE | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JGS34J7L9I |
| Rxcui | 387013, 751612, 751618, 827073 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-483-30 | Nebivolol | 30 in 1 BOTTLE | TABLET | 30 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-483 | NEBIVOLOL TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.] | 9 | Current NDC, Legacy NDC, 1 package rows | 20241228_c9d8edb5-5312-ad38-e053-2995a90a7154.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-483-30 | 51407048330 | 30 TABLET in 1 BOTTLE (51407-483-30) | 30 tablet | 2021-09-17 | 0000-00-00 | No | No | Current |