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Fenofibrate

NDC 69238-1260, Fenofibrate, tablet, from Amneal Pharmaceuticals NY LLC.

Product NDC
69238-1260
Status
Listed
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209951
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1260 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE48 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
69238-1260-96923812600990 TABLET in 1 BOTTLE (69238-1260-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/283e754e-6ffa-4d6a-882f-9bbb3cbc8ca8

Use it

Look up 69238-1260 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1260 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69238-1260. 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.