Carvedilol
- Product NDC
- 70934-910
- 11-digit product format
- 709340910
- Labeler code
- 70934
- Product ID
- 70934-910_f161a8e2-b6e0-27d7-e053-2995a90aa01c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA078384
- Marketing category
- ANDA
- Marketing start
- 2021-10-12
- Marketing end
- 2023-07-31
- 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
- 0000-00-00
- 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 |
|---|
| 70934-910-30 | 70934091030 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-910-30) | 2022-05-23 | 0000-00-00 | No | No | Current |
| 70934-910-60 | 70934091060 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-910-60) | 2021-10-12 | 0000-00-00 | No | No | Current |
| 70934-910-90 | 70934091090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-910-90) | 2021-10-13 | 0000-00-00 | No | No | Current |