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Fenofibrate

NDC 69315-290, Fenofibrate, tablet, film coated, from Leading Pharma, LLC.

Product NDC
69315-290
Status
Listed
Labeler
Leading Pharma, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210606
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69315-290 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE160 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
69315-290-0569315029005500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05)
69315-290-096931502900990 TABLET, FILM COATED in 1 BOTTLE (69315-290-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f73a40ef-1513-4a07-a5a9-51efb30bf560

Use it

Look up 69315-290 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69315-290 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69315-290. 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.