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FENOFIBRATE

NDC 71335-1756, FENOFIBRATE, tablet, from Bryant Ranch Prepack.

Product NDC
71335-1756
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213864
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1756 \
  -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
71335-1756-17133517560130 TABLET in 1 BOTTLE (71335-1756-1)
71335-1756-27133517560290 TABLET in 1 BOTTLE (71335-1756-2)
71335-1756-37133517560360 TABLET in 1 BOTTLE (71335-1756-3)
71335-1756-47133517560428 TABLET in 1 BOTTLE (71335-1756-4)
71335-1756-571335175605100 TABLET in 1 BOTTLE (71335-1756-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d34f9fa3-39ae-4b8e-8f29-0d5c655c50b5

Use it

Look up 71335-1756 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1756 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-1756. 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.