Ezetimibe — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

EZETIMIBE

Base moiety

EZETIMIBE

RxNorm CUI

476345

UNII

EOR26LQQ24

Medication products

9

Brand names

5

Dosage forms

4

FAERS reports

262,992 · not a risk measure

Products containing this ingredient

Source: NDC Directory 9 products

bempedoic acid and ezetimibe Tablet, Film Coated
2 NDC
Ezetimibe Powder
17 NDC
Ezetimibe Granule
1 NDC
Ezetimibe (Form-B) Powder
1 NDC
Nexlizet Bempedoic Acid and Ezetimibe · Tablet, Film Coated
Rx NDA 2 recalls 1 NDC
Zetia Ezetimibe · Tablet
Rx NDA TE AB 1 NDC
Ezetimibe Tablet
Rx ANDA TE AB 42 NDC
Ezetimibe and Simvastatin Tablet
Rx ANDA TE AB 9 recalls 36 NDC
VYTORIN ezetimibe and simvastatin · Tablet
Rx NDA TE AB 4 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Tablet	4	Zetia, Ezetimibe, Ezetimibe and Simvastatin, VYTORIN
TABLET, Film Coated	2	bempedoic acid and ezetimibe, Nexlizet
Powder	2	Ezetimibe, Ezetimibe (Form-B)
Granule	1	Ezetimibe

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals