NDC 68788-4006 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-4006

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090856
Marketed since
August 8, 2025
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (4)

Package NDCDescriptionSince
68788-4006-1100 TABLET in 1 BOTTLE (68788-4006-1)Aug 8, 2025
68788-4006-330 TABLET in 1 BOTTLE (68788-4006-3)Aug 8, 2025
68788-4006-660 TABLET in 1 BOTTLE (68788-4006-6)Aug 8, 2025
68788-4006-990 TABLET in 1 BOTTLE (68788-4006-9)Aug 8, 2025

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