NDC 70756-215 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70756-215

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Lifestar Pharma LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213864
Marketed since
September 10, 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 (2)

Package NDCDescriptionSince
70756-215-51500 TABLET in 1 BOTTLE (70756-215-51)Sep 10, 2020
70756-215-9090 TABLET in 1 BOTTLE (70756-215-90)Sep 10, 2020

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