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Fenofibrate

NDC 68071-3542, Fenofibrate, tablet, film coated, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-3542
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
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/68071-3542 \
  -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
68071-3542-96807135420990 TABLET, FILM COATED in 1 BOTTLE (68071-3542-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0b4e90dd-646b-afec-e063-6294a90a598e

Use it

Look up 68071-3542 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3542 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3542. 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.