FENOFIBRIC ACID
NDC 59651-217, FENOFIBRIC ACID, capsule, delayed release, from Aurobindo Pharma Limited.
- Product NDC
- 59651-217
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212598
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-217 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FENOFIBRIC ACID135 mg/1
Pharmacologic classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59651-217-90 | 59651021790 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-217-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/9ad201de-fa62-4c49-bc61-ee09b9ba434cNADAC price for package 59651021790
GET /v1/drugs/nadac/59651021790
Use it
Look up 59651-217 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-217 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-217. 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.