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Fenofibrate

NDC 48433-040, fenofibrate, tablet, film coated, from Safecor Health, LLC.

Product NDC
48433-040
Status
Listed
Labeler
Safecor Health, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202856
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/48433-040 \
  -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
48433-040-2048433004020100 BLISTER PACK in 1 CARTON (48433-040-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-040-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9cc2038d-750e-42dc-b818-c5642cf6a5ad

Use it

Look up 48433-040 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/48433-040 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 48433-040. 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.