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Fenofibrate

NDC 33342-339, Fenofibrate, tablet, from Macleods Pharmaceuticals Limited.

Product NDC
33342-339
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210248
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-339 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE48 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
33342-339-073334203390730 TABLET in 1 BOTTLE (33342-339-07)
33342-339-103334203391090 TABLET in 1 BOTTLE (33342-339-10)
33342-339-123334203391210 BLISTER PACK in 1 CARTON (33342-339-12) / 10 TABLET in 1 BLISTER PACK
33342-339-1533342033915500 TABLET in 1 BOTTLE (33342-339-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e8b9d1f5-0541-424f-b1d4-bef6381aa934

Use it

Look up 33342-339 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-339 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-339. 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.