NDC 82009-060 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC82009-060

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
QUALLENT PHARMACEUTICALS HEALTH LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA205118
Marketed since
November 18, 2022
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 (1)

Package NDCDescriptionSince
82009-060-9090 TABLET, COATED in 1 BOTTLE (82009-060-90)Nov 18, 2022

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