Carvedilol
- Product NDC
- 68788-8151
- 11-digit product format
- 687888151
- Labeler code
- 68788
- Product ID
- 68788-8151_991683d3-c725-4821-8fdd-68c1b080a3fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078251
- Marketing category
- ANDA
- Marketing start
- 2022-03-04
- 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
- 2023-12-31
- 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 |
|---|
| 68788-8151-1 | 68788815101 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8151-1) | 2022-03-04 | 0000-00-00 | No | No | Current |
| 68788-8151-3 | 68788815103 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8151-3) | 2022-03-04 | 0000-00-00 | No | No | Current |
| 68788-8151-6 | 68788815106 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8151-6) | 2022-03-04 | 0000-00-00 | No | No | Current |
| 68788-8151-9 | 68788815109 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8151-9) | 2022-03-04 | 0000-00-00 | No | No | Current |