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Fenofibrate

NDC 43975-305, Fenofibrate, capsule, from ANI Pharmaceuticals, Inc..

Product NDC
43975-305
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209504
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43975-305 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE134 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
43975-305-1043975030510100 CAPSULE in 1 BOTTLE (43975-305-10)
43975-305-5043975030550500 CAPSULE in 1 BOTTLE (43975-305-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c740f57c-cac5-4526-a5a9-aaab65b1caf6

  • NADAC price for package 43975030510

    GET /v1/drugs/nadac/43975030510

Use it

Look up 43975-305 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43975-305 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43975-305. 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.