NDC 50090-3887 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC50090-3887

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
A-S Medication Solutions
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA205118
Marketed since
May 5, 2016
Listing expires
December 31, 2027
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (1)

Package NDCDescriptionSince
50090-3887-090 TABLET, COATED in 1 BOTTLE (50090-3887-0)Nov 30, 2018

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