nebivolol
- Product NDC
- 0904-7189
- 11-digit product format
- 009047189
- Labeler code
- 0904
- Product ID
- 0904-7189_13c6911b-c653-4fa9-87ea-3e505bf3ba34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA203966
- Marketing category
- ANDA
- Marketing start
- 2018-03-02
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7189 | NEBIVOLOL TABLET [MAJOR PHARMACEUTICALS] | 7 | Legacy NDC | 20250321_1a3b660c-1a31-4240-9d7b-1e04225459f3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7189-04 | 00904718904 | 30 BLISTER PACK in 1 CARTON (0904-7189-04) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2018-03-02 | 0000-00-00 | No | No | Current |