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Fenofibrate

NDC 60505-3120, Fenofibrate, capsule, from Apotex Corp..

Product NDC
60505-3120
Status
Listed
Labeler
Apotex Corp.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202252
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60505-3120 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE43 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
60505-3120-160505312001100 CAPSULE in 1 BOTTLE (60505-3120-1)
60505-3120-36050531200330 CAPSULE in 1 BOTTLE (60505-3120-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/68024459-987a-9cf4-f539-4959093bc9f0

  • NADAC price for package 60505312003

    GET /v1/drugs/nadac/60505312003

Use it

Look up 60505-3120 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60505-3120 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60505-3120. 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.