Carvedilol
- Product NDC
- 71335-1533
- 11-digit product format
- 713351533
- Labeler code
- 71335
- Product ID
- 71335-1533_06540a82-d48f-46df-bf2c-04e8332ba9ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078251
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- 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 |
|---|
| 71335-1533-1 | 71335153301 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1533-1) | 2011-08-10 | No | No | Historical |
| 71335-1533-2 | 71335153302 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1533-2) | 2011-08-10 | No | No | Historical |
| 71335-1533-3 | 71335153303 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1533-3) | 2011-08-10 | No | No | Historical |
| 71335-1533-4 | 71335153304 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1533-4) | 2011-08-10 | No | No | Historical |
| 71335-1533-5 | 71335153305 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1533-5) | 2011-08-10 | No | No | Historical |
| 71335-1533-6 | 71335153306 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1533-6) | 2011-08-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Carvedilol | Bryant Ranch Prepack | 2023-12-08 | HUMAN PRESCRIPTION DRUG LABEL | 9 |