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Fenofibrate

NDC 65862-769, Fenofibrate, tablet, coated, from Aurobindo Pharma Limited.

Product NDC
65862-769
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205118
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-769 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE145 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
65862-769-0165862076901100 TABLET, COATED in 1 BOTTLE (65862-769-01)
65862-769-0565862076905500 TABLET, COATED in 1 BOTTLE (65862-769-05)
65862-769-786586207697810 BLISTER PACK in 1 CARTON (65862-769-78) / 10 TABLET, COATED in 1 BLISTER PACK (65862-769-10)
65862-769-906586207699090 TABLET, COATED in 1 BOTTLE (65862-769-90)
65862-769-99658620769991000 TABLET, COATED in 1 BOTTLE (65862-769-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/84fcea7a-05ed-44c2-98fa-7e87b28d2261

  • NADAC price for package 65862076990

    GET /v1/drugs/nadac/65862076990

Use it

Look up 65862-769 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-769 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-769. 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.