nebivolol
- Product NDC
- 13668-355
- 11-digit product format
- 136680355
- Labeler code
- 13668
- Product ID
- 13668-355_dd21623c-b76b-415e-9be7-d423f6719096
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA203966
- Marketing category
- ANDA
- Marketing start
- 2018-03-02
- Marketing end
- 0000-00-00
- Substance
- NEBIVOLOL HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 13668-355 | NEBIVOLOL TABLET [TORRENT PHARMACEUTICALS LIMITED] | 18 | Legacy NDC | 20241213_3e3dc363-731f-4115-b685-a17620dd2034.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13668-355-01 | 13668035501 | 100 TABLET in 1 BOTTLE (13668-355-01) | 100 tablet | 2021-08-19 | 0000-00-00 | No | No | Current |
| 13668-355-05 | 13668035505 | 500 TABLET in 1 BOTTLE (13668-355-05) | 500 tablet | 2018-03-02 | 0000-00-00 | No | No | Current |
| 13668-355-30 | 13668035530 | 30 TABLET in 1 BOTTLE (13668-355-30) | 30 tablet | 2018-03-02 | 0000-00-00 | No | No | Current |
| 13668-355-74 | 13668035574 | 100 TABLET in 1 CARTON (13668-355-74) | 100 tablet | 2021-08-19 | 0000-00-00 | No | No | Current |
| 13668-355-90 | 13668035590 | 90 TABLET in 1 BOTTLE (13668-355-90) | 90 tablet | 2021-06-17 | 0000-00-00 | No | No | Current |