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Fenofibrate

NDC 69097-459, FENOFIBRATE, tablet, from Cipla USA Inc..

Product NDC
69097-459
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208709
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-459 \
  -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
69097-459-026909704590230 TABLET in 1 BOTTLE (69097-459-02)
69097-459-056909704590590 TABLET in 1 BOTTLE (69097-459-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f8f09ab1-74db-4123-b85a-6337dc2582a0

  • NADAC price for package 69097045905

    GET /v1/drugs/nadac/69097045905

Use it

Look up 69097-459 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-459 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-459. 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.