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Fenofibrate

NDC 33342-348, Fenofibrate, tablet, from Macleods Pharmaceuticals Limited.

Product NDC
33342-348
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210379
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-348 \
  -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
33342-348-103334203481090 TABLET in 1 CONTAINER (33342-348-10)
33342-348-123334203481210 BLISTER PACK in 1 CARTON (33342-348-12) / 10 TABLET in 1 BLISTER PACK
33342-348-1533342034815500 TABLET in 1 CONTAINER (33342-348-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a504c42a-b629-4a21-a716-084962266b48

Use it

Look up 33342-348 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-348 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-348. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.