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Fenofibric Acid

NDC 0115-1325, FENOFIBRIC ACID, capsule, delayed release, from Amneal Pharmaceuticals of New York LLC.

Product NDC
0115-1325
Status
Listed
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200264
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0115-1325 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRIC ACID135 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
0115-1325-100011513251090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1325-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e73404c5-e0ee-48e9-8b09-7a00d7e18e6c

  • NADAC price for package 00115132510

    GET /v1/drugs/nadac/00115132510

Use it

Look up 0115-1325 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0115-1325 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0115-1325. 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.