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FENOFIBRATE

NDC 73352-102, fenofibrate, tablet, from Trifluent Pharma LLC.

Product NDC
73352-102
Status
Listed
Labeler
Trifluent Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217732
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73352-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE120 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
73352-102-017335201020190 TABLET in 1 BOTTLE (73352-102-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3c3539e4-bc4a-8152-e063-6294a90ab55c

  • NADAC price for package 73352010201

    GET /v1/drugs/nadac/73352010201

Use it

Look up 73352-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73352-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73352-102. 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.