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FENOFIBRATE

NDC 71335-0891, FENOFIBRATE, tablet, from Bryant Ranch Prepack.

Product NDC
71335-0891
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208709
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0891 \
  -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
71335-0891-17133508910130 TABLET in 1 BOTTLE (71335-0891-1)
71335-0891-27133508910290 TABLET in 1 BOTTLE (71335-0891-2)
71335-0891-37133508910328 TABLET in 1 BOTTLE (71335-0891-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b11f1c74-23da-4273-b504-0a2ca22c4b5a

Use it

Look up 71335-0891 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0891 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0891. 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.