CARVEDILOL
- Product NDC
- 68071-3970
- 11-digit product format
- 680713970
- Labeler code
- 68071
- Product ID
- 68071-3970_4bbf366b-77c8-fc66-e063-6394a90aebf4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CARVEDILOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA078165
- Marketing category
- ANDA
- Marketing start
- 2021-07-29
- Substance
- CARVEDILOL
- Active strength
- 3.125 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
- 2027-12-31
- 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 |
|---|
| 68071-3970-6 | 68071397006 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3970-6) | 2026-02-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| CARVEDILOL | NuCare Pharmaceuticals, Inc. | 2026-02-26 | HUMAN PRESCRIPTION DRUG LABEL | 1 |