Plavix
NDC 0024-1332, clopidogrel, tablet, film coated, from Sanofi-Aventis U.S. LLC.
- Product NDC
- 0024-1332
- Status
- Listed
- Labeler
- Sanofi-Aventis U.S. LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA020839
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0024-1332 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CLOPIDOGREL BISULFATE300 mg/1
Pharmacologic classes
Cytochrome P450 2C8 Inhibitors [MoA]; Decreased Platelet Aggregation [PE]; P2Y12 Platelet Inhibitor [EPC]; P2Y12 Receptor Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0024-1332-30 | 00024133230 | 3 BLISTER PACK in 1 CARTON (0024-1332-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/de8b0b67-eb25-4684-83b5-7ad785314227
Use it
Look up 0024-1332 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0024-1332 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0024-1332. 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.