NDC 71335-2123 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2123

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Bryant Ranch Prepack
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 (5)

Package NDCDescriptionSince
71335-2123-130 TABLET in 1 BOTTLE (71335-2123-1)Aug 31, 2022
71335-2123-290 TABLET in 1 BOTTLE (71335-2123-2)Aug 24, 2022
71335-2123-328 TABLET in 1 BOTTLE (71335-2123-3)Apr 3, 2024
71335-2123-418 TABLET in 1 BOTTLE (71335-2123-4)Apr 3, 2024
71335-2123-560 TABLET in 1 BOTTLE (71335-2123-5)Nov 22, 2023

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