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Fenofibrate

NDC 42858-660, Fenofibrate, tablet, film coated, from Rhodes Pharmaceuticals LLC.

Product NDC
42858-660
Status
Listed
Labeler
Rhodes Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076433
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42858-660 \
  -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
42858-660-454285806604590 TABLET, FILM COATED in 1 BOTTLE (42858-660-45)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5e7b79ab-9df0-4bbf-b7a4-a44aec203555

  • NADAC price for package 42858066045

    GET /v1/drugs/nadac/42858066045

Use it

Look up 42858-660 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42858-660 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42858-660. 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.