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Fenofibrate

NDC 68071-2369, Fenofibrate, tablet, coated, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2369
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205118
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2369 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE48 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
68071-2369-96807123690990 TABLET, COATED in 1 BOTTLE (68071-2369-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bdc2211e-6d65-1500-e053-2a95a90ab145

Use it

Look up 68071-2369 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2369 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2369. 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.