NDC 43975-305 – Fenofibrate

Fenofibrate 134 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC43975-305

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA209504
Marketed since
May 1, 2018
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 (2)

Package NDCDescriptionSince
43975-305-10100 CAPSULE in 1 BOTTLE (43975-305-10)May 1, 2018
43975-305-50500 CAPSULE in 1 BOTTLE (43975-305-50)May 1, 2018

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