NDC 70518-2907 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-2907

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213864
Marketed since
October 13, 2020
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
70518-2907-190 TABLET in 1 BOTTLE, PLASTIC (70518-2907-1)Jan 13, 2021

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