NDC 71335-3092 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3092

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210859
Marketed since
July 26, 2022
Listing expires
December 31, 2027
Pharmacologic class
Dietary Cholesterol Absorption Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ezetimibe →

Package NDC codes (5)

Package NDCDescriptionSince
71335-3092-130 TABLET in 1 BOTTLE (71335-3092-1)Feb 17, 2026
71335-3092-290 TABLET in 1 BOTTLE (71335-3092-2)Feb 17, 2026
71335-3092-328 TABLET in 1 BOTTLE (71335-3092-3)Feb 17, 2026
71335-3092-418 TABLET in 1 BOTTLE (71335-3092-4)Feb 17, 2026
71335-3092-560 TABLET in 1 BOTTLE (71335-3092-5)Feb 17, 2026

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