United States · FDA National Drug Code directory

Fenofibrate

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
35561-343_49fce536-9885-9845-e063-6394a90af375
Product NDC
35561-343
Form
TABLET, FILM COATED
Composition / generic term
Fenofibrate
Labeler
Bostal LLC
Marketing category
ANDA
Marketing start / end (source format)
20190630
Source listing expiry
20271231

Source-listed ingredients

  • FENOFIBRATE — 54 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 63784 TABLET, FILM COATED in 1 BOX (35561-343-00) · 35561-343-00
  • 90 TABLET, FILM COATED in 1 BOTTLE (35561-343-11) · 35561-343-11
  • 500 TABLET, FILM COATED in 1 BOTTLE (35561-343-13) · 35561-343-13

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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Fenofibrate — United States | Molindra Medicines