Carvedilol
- Product NDC
- 60760-376
- 11-digit product format
- 607600376
- Labeler code
- 60760
- Product ID
- 60760-376_a449a3b6-1eaa-3d0f-e053-2a95a90a39df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA078384
- Marketing category
- ANDA
- Marketing start
- 2020-04-23
- 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
- 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 |
|---|
| 60760-376-60 | 60760037660 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-376-60) | 2020-04-23 | 0000-00-00 | No | No | Current |