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FENOFIBRATE

NDC 72789-410, FENOFIBRATE, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-410
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/72789-410 \
  -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
72789-410-307278904103030 TABLET in 1 BOTTLE, PLASTIC (72789-410-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/35ba17d9-0dd7-4f15-8f74-be5fd15f1917

Use it

Look up 72789-410 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-410 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-410. 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.