Carvedilol
- Product NDC
- 70934-653
- 11-digit product format
- 709340653
- Labeler code
- 70934
- Product ID
- 70934-653_aa7d768e-b081-f1b5-e053-2995a90a6173
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA078227
- Marketing category
- ANDA
- Marketing start
- 2020-04-01
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 70934-653-30 | 70934065330 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-653-30) | 2020-04-14 | 0000-00-00 | No | No | Current |
| 70934-653-90 | 70934065390 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-653-90) | 2020-04-01 | 0000-00-00 | No | No | Current |