Fenofibrate
NDC 42291-427, Fenofibrate, tablet, film coated, from AvKARE.
- Product NDC
- 42291-427
- Status
- Listed
- Labeler
- AvKARE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207803
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42291-427 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FENOFIBRATE160 mg/1
Pharmacologic classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42291-427-50 | 42291042750 | 500 TABLET, FILM COATED in 1 BOTTLE (42291-427-50) |
| 42291-427-90 | 42291042790 | 90 TABLET, FILM COATED in 1 BOTTLE (42291-427-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f669f231-98b9-5014-e053-2a95a90a4e4c
Use it
Look up 42291-427 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42291-427 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42291-427. 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.