United States · FDA National Drug Code directory

Fenofibric acid

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
33342-294_94a44831-98b3-41d4-89da-89a43b25d15f
Product NDC
33342-294
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Fenofibric acid
Labeler
Macleods Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20240226
Source listing expiry
20261231

Source-listed ingredients

  • CHOLINE FENOFIBRATE — 45 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-294-10) · 33342-294-10
  • 10 BLISTER PACK in 1 CARTON (33342-294-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK · 33342-294-12

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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