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Fenofibrate

NDC 62332-539, Fenofibrate, tablet, film coated, from Alembic Pharmaceuticals Inc..

Product NDC
62332-539
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209660
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62332-539 \
  -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
62332-539-906233205399090 TABLET, FILM COATED in 1 BOTTLE (62332-539-90)
62332-539-91623320539911000 TABLET, FILM COATED in 1 BOTTLE (62332-539-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4387adac-eea0-40c5-8111-1b70e0d98d7e

Use it

Look up 62332-539 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-539 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-539. 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.