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
- 33342-339_ab7aad70-2879-4260-831e-cbfbe8be73b2
- Product NDC
- 33342-339
- Form
- TABLET
- Composition / generic term
- Fenofibrate
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241113
- Source listing expiry
- 20261231
Source-listed ingredients
- FENOFIBRATE — 48 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (33342-339-07) · 33342-339-07
- 90 TABLET in 1 BOTTLE (33342-339-10) · 33342-339-10
- 10 BLISTER PACK in 1 CARTON (33342-339-12) / 10 TABLET in 1 BLISTER PACK · 33342-339-12
- 500 TABLET in 1 BOTTLE (33342-339-15) · 33342-339-15
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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