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FENOFIBRATE

NDC 42385-936, FENOFIBRATE, tablet, film coated, from Laurus Labs Limited.

Product NDC
42385-936
Status
Listed
Labeler
Laurus Labs Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210606
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42385-936 \
  -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
42385-936-0542385093605500 TABLET, FILM COATED in 1 BOTTLE (42385-936-05)
42385-936-11423850936111000 TABLET, FILM COATED in 1 BOTTLE (42385-936-11)
42385-936-304238509363030 TABLET, FILM COATED in 1 BOTTLE (42385-936-30)
42385-936-904238509369090 TABLET, FILM COATED in 1 BOTTLE (42385-936-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8e58c13a-8088-4fed-86cc-52530de5aa45

Use it

Look up 42385-936 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42385-936 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42385-936. 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.