NEBIVOLOL
- Product NDC
- 0904-7499
- 11-digit product format
- 009047499
- Labeler code
- 0904
- Product ID
- 0904-7499_2562c60f-8883-417d-a6db-01f4f243b199
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA212682
- Marketing category
- ANDA
- Marketing start
- 2025-02-24
- Substance
- NEBIVOLOL
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 030Y90569U |
| 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 |
|---|
| 0904-7499-04 | NEBIVOLOL | 1 in 1 BLISTER PACK | TABLET | 1 | | 4 |
| 0904-7499-04 | NEBIVOLOL | 30 in 1 CARTON | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7499 | NEBIVOLOL TABLET [MAJOR PHARMACEUTICALS] | 2 | Current NDC, 2 package rows | 20250410_3e9e1048-b5ea-4d6a-9363-3ee0d059e088.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 |
|---|
| 0904-7499-04 | 00904749904 | 30 BLISTER PACK in 1 CARTON (0904-7499-04) / 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2025-02-24 | No | No | Historical |