Fenofibrate
NDC 70518-4721, Fenofibrate, tablet, film coated, from REMEDYREPACK INC..
- Product NDC
- 70518-4721
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216798
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4721 \ -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 |
|---|---|---|
| 70518-4721-0 | 70518472100 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4721-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b6b5d74d-d418-4ada-8ccd-592b0f57b2ff
Use it
Look up 70518-4721 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4721 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4721. 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.