Carvedilol
- Product NDC
- 68788-7458
- 11-digit product format
- 687887458
- Labeler code
- 68788
- Product ID
- 68788-7458_d0a9ad26-e55f-4c6a-a334-1596ac88a081
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078251
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 3 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7458-1 | 68788745801 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7458-1) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7458-3 | 68788745803 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7458-3) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7458-6 | 68788745806 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7458-6) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7458-8 | 68788745808 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7458-8) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7458-9 | 68788745809 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7458-9) | 2019-12-27 | 0000-00-00 | No | No | Current |