NDC 71335-0684 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0684

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208803
Marketed since
June 12, 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
71335-0684-130 TABLET in 1 BOTTLE (71335-0684-1)Mar 2, 2018
71335-0684-290 TABLET in 1 BOTTLE (71335-0684-2)Feb 12, 2018
71335-0684-328 TABLET in 1 BOTTLE (71335-0684-3)Jul 9, 2024
71335-0684-418 TABLET in 1 BOTTLE (71335-0684-4)Jul 9, 2024
71335-0684-560 TABLET in 1 BOTTLE (71335-0684-5)Feb 17, 2023

Other Ezetimibe products