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FENOFIBRATE

NDC 46708-361, FENOFIBRATE, tablet, film coated, from Alembic Pharmaceuticals Limited.

Product NDC
46708-361
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210476
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-361 \
  -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
46708-361-304670803613030 TABLET, FILM COATED in 1 BOTTLE (46708-361-30)
46708-361-7146708036171500 TABLET, FILM COATED in 1 BOTTLE (46708-361-71)
46708-361-904670803619090 TABLET, FILM COATED in 1 BOTTLE (46708-361-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ddafb483-bae5-49bf-845d-67c29e6dc12d

Use it

Look up 46708-361 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-361 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-361. 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.