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fenofibrate

NDC 42385-951, fenofibrate, tablet, from Laurus Labs Limited.

Product NDC
42385-951
Status
Listed
Labeler
Laurus Labs Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211122
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42385-951 \
  -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
42385-951-11423850951111000 TABLET in 1 BOTTLE (42385-951-11)
42385-951-304238509513030 TABLET in 1 BOTTLE (42385-951-30)
42385-951-904238509519090 TABLET in 1 BOTTLE (42385-951-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0da6d56e-1ed6-437d-b88d-16b014d1889a

Use it

Look up 42385-951 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42385-951 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42385-951. 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.