Carvedilol
- Product NDC
- 68788-7883
- 11-digit product format
- 687887883
- Labeler code
- 68788
- Product ID
- 68788-7883_6fd221f3-f96f-499a-9e4f-386aab3e5057
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmacdeuticals Inc
- Application
- ANDA078384
- Marketing category
- ANDA
- Marketing start
- 2021-03-26
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 6 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0K47UL67F2 | CARVEDILOL | 72956-09-3 | CARVEDILOL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7883-1 | 68788788301 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-1) | 2021-03-26 | 0000-00-00 | No | No | Current |
| 68788-7883-3 | 68788788303 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-3) | 2021-03-26 | 0000-00-00 | No | No | Current |
| 68788-7883-6 | 68788788306 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-6) | 2021-03-26 | 0000-00-00 | No | No | Current |
| 68788-7883-8 | 68788788308 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-8) | 2021-03-26 | 0000-00-00 | No | No | Current |
| 68788-7883-9 | 68788788309 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-9) | 2021-03-26 | 0000-00-00 | No | No | Current |