Carvedilol
- Product NDC
- 82804-225
- 11-digit product format
- 828040225
- Labeler code
- 82804
- Product ID
- 82804-225_da2696ba-f4be-4626-9abe-fe33f36361b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076373
- Marketing category
- ANDA
- Marketing start
- 2007-09-06
- Substance
- CARVEDILOL
- Active strength
- 12.5 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 82804-225-90 | 82804022590 | 90 TABLET, FILM COATED in 1 BOTTLE (82804-225-90) | 2025-05-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Carvedilol | Proficient Rx LP | 2025-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |