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FENOFIBRATE

NDC 0115-5522, FENOFIBRATE, tablet, from Amneal Pharmaceuticals of New York LLC.

Product NDC
0115-5522
Status
Listed
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076509
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0115-5522 \
  -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
0115-5522-0100115552201100 TABLET in 1 BOTTLE (0115-5522-01)
0115-5522-0200115552202500 TABLET in 1 BOTTLE (0115-5522-02)
0115-5522-03001155522031000 TABLET in 1 BOTTLE (0115-5522-03)
0115-5522-100011555221090 TABLET in 1 BOTTLE (0115-5522-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fa08cf6a-d306-4979-9b23-ac7febf4fd12

  • NADAC price for package 00115552202

    GET /v1/drugs/nadac/00115552202

  • NADAC price for package 00115552210

    GET /v1/drugs/nadac/00115552210

Use it

Look up 0115-5522 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0115-5522 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0115-5522. 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.