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FENOFIBRATE

NDC 60219-5522, FENOFIBRATE, tablet, from Amneal Pharmaceuticals LLC.

Product NDC
60219-5522
Status
Listed
Labeler
Amneal Pharmaceuticals 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/60219-5522 \
  -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
60219-5522-560219552205500 TABLET in 1 BOTTLE (60219-5522-5)
60219-5522-96021955220990 TABLET in 1 BOTTLE (60219-5522-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/65f5dcad-5073-4347-9ec9-e7f350b134c4

  • NADAC price for package 60219552205

    GET /v1/drugs/nadac/60219552205

  • NADAC price for package 60219552209

    GET /v1/drugs/nadac/60219552209

Use it

Look up 60219-5522 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60219-5522 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60219-5522. 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.