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Fenofibrate

NDC 50090-5796, fenofibrate, tablet, film coated, from A-S Medication Solutions.

Product NDC
50090-5796
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200884
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-5796 \
  -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
50090-5796-05009057960090 TABLET, FILM COATED in 1 BOTTLE (50090-5796-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/06870192-c92a-40c7-a619-efda0c006301

Use it

Look up 50090-5796 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-5796 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-5796. 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.