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Fenofibrate

NDC 55111-395, Fenofibrate, capsule, from Dr. Reddy's Laboratories Limited.

Product NDC
55111-395
Status
Listed
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090859
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-395 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE130 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
55111-395-0155111039501100 CAPSULE in 1 BOTTLE (55111-395-01)
55111-395-305511103953030 CAPSULE in 1 BOTTLE (55111-395-30)
55111-395-905511103959090 CAPSULE in 1 BOTTLE (55111-395-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/16ea8ce4-8c1c-4111-509e-86aa688d89a0

Use it

Look up 55111-395 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-395 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-395. 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.