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Fenofibrate

NDC 46708-351, Fenofibrate, tablet, film coated, from Alembic Pharmaceuticals Limited.

Product NDC
46708-351
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213252
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-351 \
  -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
46708-351-304670803513030 TABLET, FILM COATED in 1 BOTTLE (46708-351-30)
46708-351-7146708035171500 TABLET, FILM COATED in 1 BOTTLE (46708-351-71)
46708-351-904670803519090 TABLET, FILM COATED in 1 BOTTLE (46708-351-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/65ca643c-3b31-4e53-bc06-0e11418baf7d

Use it

Look up 46708-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-351. 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.