CARVEDILOL
- Product NDC
- 68788-8177
- 11-digit product format
- 687888177
- Labeler code
- 68788
- Product ID
- 68788-8177_29e5b8be-74c1-46de-8c6a-ec1950594a71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CARVEDILOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078165
- Marketing category
- ANDA
- Marketing start
- 2022-04-28
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 6 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 |
|---|
| 68788-8177-3 | 68788817703 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8177-3) | 2022-04-28 | 0000-00-00 | No | No | Current |
| 68788-8177-6 | 68788817706 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8177-6) | 2022-04-28 | 0000-00-00 | No | No | Current |
| 68788-8177-9 | 68788817709 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8177-9) | 2022-04-28 | 0000-00-00 | No | No | Current |