Carvedilol
- Product NDC
- 70934-874
- 11-digit product format
- 709340874
- Labeler code
- 70934
- Product ID
- 70934-874_c7ccf8ac-79c7-984c-e053-2a95a90a0d1f
- 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
- 2021-07-22
- Marketing end
- 2023-08-31
- 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
- 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 |
|---|
| 70934-874-30 | 70934087430 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-874-30) | 2021-07-22 | 2023-08-31 | No | No | Current |
| 70934-874-60 | 70934087460 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-874-60) | 2021-10-08 | 2023-05-31 | No | No | Current |
| 70934-874-96 | 70934087496 | 96 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-874-96) | 2021-12-02 | 2023-04-30 | No | No | Current |