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Fenofibrate

NDC 43598-909, FENOFIBRATE, tablet, film coated, from Dr. Reddy's Laboratories Inc..

Product NDC
43598-909
Status
Listed
Labeler
Dr. Reddy's Laboratories Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210670
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-909 \
  -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
43598-909-904359809099090 TABLET, FILM COATED in 1 BOTTLE (43598-909-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9e69d844-5ded-46b6-8321-c420e8b37a63

Use it

Look up 43598-909 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-909 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-909. 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.