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Fenofibrate

NDC 31722-596, Fenofibrate, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-596
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204598
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-596 \
  -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
31722-596-303172205963030 TABLET, FILM COATED in 1 BOTTLE (31722-596-30)
31722-596-313172205963170 TABLET, FILM COATED in 1 BLISTER PACK (31722-596-31)
31722-596-3231722059632100 TABLET, FILM COATED in 1 BLISTER PACK (31722-596-32)
31722-596-903172205969090 TABLET, FILM COATED in 1 BOTTLE (31722-596-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/38f43148-4ca0-402a-ba39-8ee5011a7907

  • NADAC price for package 31722059690

    GET /v1/drugs/nadac/31722059690

Use it

Look up 31722-596 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-596 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-596. 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.