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fenofibrate

NDC 69315-288, fenofibrate, tablet, from Leading Pharma, LLC.

Product NDC
69315-288
Status
Listed
Labeler
Leading Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211122
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69315-288 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE145 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
69315-288-0569315028805500 TABLET in 1 BOTTLE (69315-288-05)
69315-288-096931502880990 TABLET in 1 BOTTLE (69315-288-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ca09372a-3c75-47c9-80a3-e08dbe243bb4

Use it

Look up 69315-288 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69315-288 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69315-288. 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.