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FENOFIBRATE

NDC 72603-841, FENOFIBRATE, tablet, from NorthStar RxLLC.

Product NDC
72603-841
Status
Listed
Labeler
NorthStar RxLLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213864
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72603-841 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE160 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
72603-841-017260308410190 TABLET in 1 BOTTLE (72603-841-01)
72603-841-0272603084102500 TABLET in 1 BOTTLE (72603-841-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3b448774-aebf-45fe-92f1-b8eca53cf09b

  • NADAC price for package 72603084101

    GET /v1/drugs/nadac/72603084101

  • NADAC price for package 72603084102

    GET /v1/drugs/nadac/72603084102

Use it

Look up 72603-841 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-841 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-841. 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.