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
- 46708-351_8250e3fe-6420-401e-af14-45662b8a7b48
- Product NDC
- 46708-351
- Form
- TABLET, FILM COATED
- Composition / generic term
- Fenofibrate
- Labeler
- Alembic Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200123
- Source listing expiry
- 20261231
Source-listed ingredients
- FENOFIBRATE — 160 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (46708-351-30) · 46708-351-30
- 500 TABLET, FILM COATED in 1 BOTTLE (46708-351-71) · 46708-351-71
- 90 TABLET, FILM COATED in 1 BOTTLE (46708-351-90) · 46708-351-90
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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