NEBIVOLOL
- Product NDC
- 50090-7301
- 11-digit product format
- 500907301
- Labeler code
- 50090
- Product ID
- 50090-7301_0b07851d-3512-4549-b39b-194211f6946f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA212682
- Marketing category
- ANDA
- Marketing start
- 2022-02-14
- Substance
- NEBIVOLOL
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 030Y90569U |
| Rxcui | 827073 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7301-1 | NEBIVOLOL | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
| 50090-7301-2 | NEBIVOLOL | 90 in 1 BOTTLE | TABLET | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7301 | NEBIVOLOL TABLET [A-S MEDICATION SOLUTIONS] | 6 | Current NDC, 2 package rows | 20241018_f20fda1a-437d-4812-b519-a26684c96c6d.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 |
|---|
| 50090-7301-1 | 50090730101 | 30 TABLET in 1 BOTTLE (50090-7301-1) | 30 tablet | 2024-10-14 | No | No | Current |
| 50090-7301-2 | 50090730102 | 90 TABLET in 1 BOTTLE (50090-7301-2) | 90 tablet | 2024-10-14 | No | No | Current |