Carvedilol
NDC 51655-034, Carvedilol, tablet, film coated, from Northwind Health Company, LLC.
- Product NDC
- 51655-034
- Status
- Listed
- Labeler
- Northwind Health Company, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077614
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51655-034 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CARVEDILOL3.125 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA]; Adrenergic beta1-Antagonists [MoA]; Adrenergic beta2-Antagonists [MoA]; alpha-Adrenergic Blocker [EPC]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51655-034-25 | 51655003425 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-25) |
| 51655-034-52 | 51655003452 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-52) |
| 51655-034-83 | 51655003483 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-83) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f2a0407c-2e05-60eb-e053-2a95a90abc99
Use it
Look up 51655-034 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51655-034 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51655-034. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.