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FENOFIBRATE

NDC 62332-361, FENOFIBRATE, tablet, film coated, from Alembic Pharmaceuticals Inc..

Product NDC
62332-361
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210476
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62332-361 \
  -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
62332-361-306233203613030 TABLET, FILM COATED in 1 BOTTLE (62332-361-30)
62332-361-7162332036171500 TABLET, FILM COATED in 1 BOTTLE (62332-361-71)
62332-361-906233203619090 TABLET, FILM COATED in 1 BOTTLE (62332-361-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5c579378-e00e-4802-b9d3-c062cf8bd9f4

  • NADAC price for package 62332036171

    GET /v1/drugs/nadac/62332036171

  • NADAC price for package 62332036190

    GET /v1/drugs/nadac/62332036190

Use it

Look up 62332-361 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-361 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-361. 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.