FENOFIBRATE
NDC 72603-840, FENOFIBRATE, tablet, from NorthStar RxLLC.
- Product NDC
- 72603-840
- Status
- Listed
- Labeler
- NorthStar RxLLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA213864
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72603-840 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FENOFIBRATE54 mg/1
Pharmacologic classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72603-840-01 | 72603084001 | 90 TABLET in 1 BOTTLE (72603-840-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3b448774-aebf-45fe-92f1-b8eca53cf09bNADAC price for package 72603084001
GET /v1/drugs/nadac/72603084001
Use it
Look up 72603-840 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72603-840 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72603-840. 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.