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Fenofibrate

NDC 35561-250, Fenofibrate, tablet, film coated, from Bostal LLC.

Product NDC
35561-250
Status
Listed
Labeler
Bostal LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208476
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/35561-250 \
  -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
35561-250-0335561025003500 TABLET, FILM COATED in 1 BOTTLE (35561-250-03)
35561-250-103556102501030 TABLET, FILM COATED in 1 BOTTLE (35561-250-10)
35561-250-113556102501190 TABLET, FILM COATED in 1 BOTTLE (35561-250-11)
35561-250-1335561025013500 TABLET, FILM COATED in 1 BOTTLE (35561-250-13)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7eb328d0-4e6f-4b24-ae85-68c2b3657569

Use it

Look up 35561-250 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/35561-250 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 35561-250. 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.