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Fenofibrate

NDC 68788-4006, Fenofibrate, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4006
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090856
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4006 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE145 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
68788-4006-168788400601100 TABLET in 1 BOTTLE (68788-4006-1)
68788-4006-36878840060330 TABLET in 1 BOTTLE (68788-4006-3)
68788-4006-66878840060660 TABLET in 1 BOTTLE (68788-4006-6)
68788-4006-96878840060990 TABLET in 1 BOTTLE (68788-4006-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2e6711e9-782d-46bd-9447-6612fe7d0fe7

Use it

Look up 68788-4006 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4006 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4006. 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.