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
- 82009-060_483b124e-3ea2-42d6-a1a8-8617df9932de
- Product NDC
- 82009-060
- Form
- TABLET, COATED
- Composition / generic term
- Fenofibrate
- Labeler
- QUALLENT PHARMACEUTICALS HEALTH LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221118
- Source listing expiry
- 20261231
Source-listed ingredients
- FENOFIBRATE — 145 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, COATED in 1 BOTTLE (82009-060-90) · 82009-060-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →