Nebivolol
- Product NDC
- 50090-5775
- 11-digit product format
- 500905775
- Labeler code
- 50090
- Product ID
- 50090-5775_0b65cf4f-b9b1-4e59-8ea9-4d4e6327ec6c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203828
- Marketing category
- ANDA
- Marketing start
- 2021-09-16
- Marketing end
- 0000-00-00
- Substance
- NEBIVOLOL HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5775 | NEBIVOLOL TABLET [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC | 20231204_15fda6ee-9332-4f20-8571-d84d46f9c498.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5775-0 | 50090577500 | 20 TABLET in 1 BOTTLE (50090-5775-0) | 20 tablet | 2021-10-07 | 0000-00-00 | No | No | Current |
| 50090-5775-1 | 50090577501 | 30 TABLET in 1 BOTTLE (50090-5775-1) | 30 tablet | 2021-10-07 | 0000-00-00 | No | No | Current |
| 50090-5775-2 | 50090577502 | 90 TABLET in 1 BOTTLE (50090-5775-2) | 90 tablet | 2021-10-07 | 0000-00-00 | No | No | Current |