Fenofibrate
NDC 0378-4390, fenofibrate, tablet, from Mylan Pharmaceuticals Inc..
- Product NDC
- 0378-4390
- Status
- Listed
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204475
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0378-4390 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FENOFIBRATE40 mg/1
Pharmacologic classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0378-4390-77 | 00378439077 | 90 TABLET in 1 BOTTLE, PLASTIC (0378-4390-77) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5b67f389-55e8-466b-82bd-5ea992f630aaNADAC price for package 00378439077
GET /v1/drugs/nadac/00378439077
Use it
Look up 0378-4390 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0378-4390 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0378-4390. 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.