fenofibrate
NDC 68462-580, fenofibrate, capsule, from Glenmark Pharmaceuticals Inc., USA.
- Product NDC
- 68462-580
- Status
- Listed
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205566
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68462-580 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FENOFIBRATE67 mg/1
Pharmacologic classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68462-580-01 | 68462058001 | 100 CAPSULE in 1 BOTTLE (68462-580-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e7204052-02cf-4b38-835b-d8754c74b2cdNADAC price for package 68462058001
GET /v1/drugs/nadac/68462058001
Use it
Look up 68462-580 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68462-580 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68462-580. 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.