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Fenofibrate

NDC 51079-599, fenofibrate, tablet, film coated, from Mylan Institutional Inc..

Product NDC
51079-599
Status
Listed
Labeler
Mylan Institutional Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202856
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51079-599 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE48 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
51079-599-2051079059920100 BLISTER PACK in 1 CARTON (51079-599-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-599-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5a90e0a4-7892-462f-9776-037d23a93b10

  • NADAC price for package 51079059920

    GET /v1/drugs/nadac/51079059920

Use it

Look up 51079-599 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51079-599 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51079-599. 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.