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Fenofibrate

NDC 82009-060, Fenofibrate, tablet, coated, from QUALLENT PHARMACEUTICALS HEALTH LLC.

Product NDC
82009-060
Status
Listed
Labeler
QUALLENT PHARMACEUTICALS HEALTH LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205118
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82009-060 \
  -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
82009-060-908200900609090 TABLET, COATED in 1 BOTTLE (82009-060-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/215a5000-9f89-47d9-b2d5-94e13f5e1767

  • NADAC price for package 82009006090

    GET /v1/drugs/nadac/82009006090

Use it

Look up 82009-060 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82009-060 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82009-060. 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.