Carvedilol
- Product NDC
- 70934-707
- 11-digit product format
- 709340707
- Labeler code
- 70934
- Product ID
- 70934-707_b7a00a71-cab3-105c-e053-2995a90aac52
- 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
- 2020-05-18
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 13 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
- 2022-12-31
- 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 |
|---|
| 70934-707-30 | 70934070730 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-707-30) | 2020-12-29 | 0000-00-00 | No | No | Current |
| 70934-707-60 | 70934070760 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-707-60) | 2020-05-18 | 0000-00-00 | No | No | Current |
| 70934-707-90 | 70934070790 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-707-90) | 2020-05-18 | 0000-00-00 | No | No | Current |
| 70934-707-96 | 70934070796 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-707-96) | 2020-05-18 | 0000-00-00 | No | No | Current |