M-EZETIMIBE TABLET

País: Canadá

Idioma: inglés

Fuente: Health Canada

Ingredientes activos:

EZETIMIBE

Disponible desde:

MANTRA PHARMA INC

Código ATC:

C10AX09

Designación común internacional (DCI):

EZETIMIBE

Dosis:

10MG

formulario farmacéutico:

TABLET

Composición:

EZETIMIBE 10MG

Vía de administración:

ORAL

Unidades en paquete:

100/500

tipo de receta:

Prescription

Área terapéutica:

CHOLESTEROL ABSORPTION INHIBITORS

Resumen del producto:

Active ingredient group (AIG) number: 0149164001; AHFS:

Estado de Autorización:

APPROVED

Fecha de autorización:

2017-08-18

Ficha técnica

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PRODUCT MONOGRAPH
PR
M-EZETIMIBE
Ezetimibe Tablets, USP
10 mg
Cholesterol Absorption Inhibitor
Mantra Pharma Inc.,
1000 du Lux, suite 201
Brossard, Quebec
J4Y 0E3
Control # 275104
Date
of
Revision:
MAY
30, 2023
Page
2
of
30
TABLE OF CONTENT
Table of Content
.....................................................................................................................................2
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................3
SUMMARY PRODUCT INFORMATION
...........................................................................................3
INDICATIONS AND CLINICAL USE
............................................................................................3
CONTRAINDICATIONS
.................................................................................................................4
WARNINGS AND PRECAUTIONS
................................................................................................4
ADVERSE REACTIONS
.................................................................................................................7
DRUG INTERACTIONS
................................................................................................................11
DOSAGE AND ADMINISTRATION
............................................................................................13
OVERDOSAGE
..............................................................................................................................14
ACTION AND CLINICAL PHARMACOLOGY
..........................................................................14
STORAGE AND STABILITY
........................................................................................................16
DOSAGE FORMS, COMPOSITION AND PACKAGING
...........................................................16
PART II: SCIENTIFIC INFORMATION
............................................................................................17
PHARMACEUTICAL INFORMATION
.......