NDC 42385-950 – fenofibrate

Fenofibrate 48 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC42385-950

Product details

Brand name
fenofibrate
Generic name
fenofibrate
Labeler
Laurus Labs Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211122
Marketed since
March 18, 2020
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 (3)

Package NDCDescriptionSince
42385-950-111000 TABLET in 1 BOTTLE (42385-950-11)Mar 18, 2020
42385-950-3030 TABLET in 1 BOTTLE (42385-950-30)Mar 18, 2020
42385-950-9090 TABLET in 1 BOTTLE (42385-950-90)Mar 18, 2020

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