Carvedilol
- Product NDC
- 70934-753
- 11-digit product format
- 709340753
- Labeler code
- 70934
- Product ID
- 70934-753_f161e26f-80f2-0c77-e053-2995a90aba08
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA078251
- Marketing category
- ANDA
- Marketing start
- 2020-05-29
- Marketing end
- 2023-08-31
- Substance
- CARVEDILOL
- Active strength
- 25 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 |
|---|
| 70934-753-96 | 70934075396 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-753-96) | 2020-05-29 | 0000-00-00 | No | No | Current |