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Fenofibrate

NDC 50090-7572, Fenofibrate, tablet, film coated, from A-S Medication Solutions.

Product NDC
50090-7572
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216798
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7572 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE54 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
50090-7572-05009075720090 TABLET, FILM COATED in 1 BOTTLE (50090-7572-0)
50090-7572-15009075720130 TABLET, FILM COATED in 1 BOTTLE (50090-7572-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/556c4800-24f6-4237-8636-3211997cbb03

Use it

Look up 50090-7572 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7572 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7572. 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.