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FENOFIBRATE

NDC 82619-102, fenofibrate, tablet, from Creekwood Pharmaceuticals LLC.

Product NDC
82619-102
Status
Listed
Labeler
Creekwood Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217732
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82619-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE120 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
82619-102-018261901020190 TABLET in 1 BOTTLE (82619-102-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/65d8aefc-7ec2-4f62-9254-5f0070c58ac2

Use it

Look up 82619-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82619-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82619-102. 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.