Carvedilol
- Product NDC
- 70934-609
- 11-digit product format
- 709340609
- Labeler code
- 70934
- Product ID
- 70934-609_ab717760-64a8-4d05-e053-2a95a90a3897
- 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
- 2020-03-07
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 70934-609-30 | 70934060930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-609-30) | 2020-03-07 | 0000-00-00 | No | No | Current |
| 70934-609-60 | 70934060960 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-609-60) | 2020-05-18 | 0000-00-00 | No | No | Current |
| 70934-609-96 | 70934060996 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-609-96) | 2020-05-19 | 0000-00-00 | No | No | Current |