NDC 59651-052 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC59651-052

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209838
Marketed since
August 25, 2017
Listing expires
December 31, 2026
Pharmacologic class
Dietary Cholesterol Absorption Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ezetimibe →

Package NDC codes (3)

Package NDCDescriptionSince
59651-052-05500 TABLET in 1 BOTTLE (59651-052-05)Aug 25, 2017
59651-052-3030 TABLET in 1 BOTTLE (59651-052-30)Aug 25, 2017
59651-052-9090 TABLET in 1 BOTTLE (59651-052-90)Aug 25, 2017

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