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Fenofibrate

NDC 69097-895, fenofibrate, capsule, from Cipla USA Inc.,.

Product NDC
69097-895
Status
Listed
Labeler
Cipla USA Inc.,
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207378
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-895 \
  -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
69097-895-026909708950230 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-02)
69097-895-0769097089507100 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-07)
69097-895-1269097089512500 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-12)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/07d47c02-ab29-4ba9-aea0-96ffbd70c0ef

Use it

Look up 69097-895 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-895 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-895. 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.