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
- 43547-431_df788edb-0354-46af-ae1f-f718f752f31b
- Product NDC
- 43547-431
- Form
- TABLET
- Composition / generic term
- fenofibrate
- Labeler
- Solco Healthcare US, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190220
- Source listing expiry
- 20261231
Source-listed ingredients
- FENOFIBRATE — 145 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (43547-431-09) · 43547-431-09
- 500 TABLET in 1 BOTTLE (43547-431-50) · 43547-431-50
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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