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Fenofibrate

NDC 59651-202, Fenofibrate, capsule, from Aurobindo Pharma Limited.

Product NDC
59651-202
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212232
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE134 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
59651-202-0159651020201100 CAPSULE in 1 BOTTLE (59651-202-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/05957860-eab3-4172-9877-455540d0c922

  • NADAC price for package 59651020201

    GET /v1/drugs/nadac/59651020201

Use it

Look up 59651-202 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-202. 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.