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Fenofibrate

NDC 51655-234, FENOFIBRATE, tablet, from Northwind Health Company, LLC.

Product NDC
51655-234
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208709
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-234 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE145 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
51655-234-525165502345230 TABLET in 1 BOTTLE, PLASTIC (51655-234-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f2b6e2a7-68d7-264d-e053-2a95a90aa9d1

Use it

Look up 51655-234 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-234 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-234. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.