fenofibrate
NDC 0615-8270, fenofibrate, tablet, from NCS HealthCare of KY, Inc dba Vangard Labs.
- Product NDC
- 0615-8270
- Status
- Listed
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210138
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8270 \ -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 |
|---|---|---|
| 0615-8270-39 | 00615827039 | 30 TABLET in 1 BLISTER PACK (0615-8270-39) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/fafbc0be-f0ba-4dcd-8aa5-89527bae5e84
Use it
Look up 0615-8270 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8270 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0615-8270. 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.