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Fenofibrate

NDC 33342-347, Fenofibrate, tablet, from Macleods Pharmaceuticals Limited.

Product NDC
33342-347
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/33342-347 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE54 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
33342-347-103334203471090 TABLET in 1 CONTAINER (33342-347-10)
33342-347-123334203471210 BLISTER PACK in 1 CARTON (33342-347-12) / 10 TABLET in 1 BLISTER PACK
33342-347-47333420347479 BLISTER PACK in 1 CARTON (33342-347-47) / 14 TABLET in 1 BLISTER PACK

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 33342-347 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-347 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-347. 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.