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Fenofibrate

NDC 69367-254, Fenofibrate, tablet, film coated, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-254
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207803
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-254 \
  -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 NDCNDC-11Package
69367-254-096936702540990 TABLET, FILM COATED in 1 BOTTLE (69367-254-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a97ebf51-4f68-4426-9958-5c59f91b1d47

  • NADAC price for package 69367025409

    GET /v1/drugs/nadac/69367025409

Use it

Look up 69367-254 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-254 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-254. 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.