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Fenofibrate

NDC 59651-576, Fenofibrate, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
59651-576
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216798
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-576 \
  -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
59651-576-905965105769090 TABLET, FILM COATED in 1 BOTTLE (59651-576-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a7cfa38f-b4db-40d3-8821-3f7c85e2727e

  • NADAC price for package 59651057690

    GET /v1/drugs/nadac/59651057690

Use it

Look up 59651-576 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-576 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-576. 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.