APO-DIPYRIDAMOLE TABLET

País: Canadá

Idioma: inglés

Fuente: Health Canada

Ingredientes activos:

DIPYRIDAMOLE

Disponible desde:

APOTEX INC

Código ATC:

B01AC07

Designación común internacional (DCI):

DIPYRIDAMOLE

Dosis:

50MG

formulario farmacéutico:

TABLET

Composición:

DIPYRIDAMOLE 50MG

Vía de administración:

ORAL

Unidades en paquete:

250ML

tipo de receta:

Prescription

Área terapéutica:

MISCELLANEOUS VASODILATATING AGENTS

Resumen del producto:

Active ingredient group (AIG) number: 0106621002; AHFS:

Estado de Autorización:

APPROVED

Fecha de autorización:

2021-08-12

Ficha técnica

Page 1 of 18
PRODUCT MONOGRAPH
PR
APO-DIPYRIDAMOLE
DIPYRIDAMOLE TABLETS USP
25, 50, 75 AND 100 MG
PR
APO-DIPYRIDAMOLE-SC
DIPYRIDAMOLE SUGAR-COATED TABLETS USP
25, 50 AND 75 MG
CORONARY VASODILATOR
INHIBITOR OF PLATELET ADHESION AND AGGREGATION
APOTEX INC.
150 SIGNET DRIVE
TORONTO, ONTARIO
DATE OF REVISION:
M9L 1T9
AUGUST 10, 2021
CONTROL NUMBER: 246833
Page 2 of 18
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.....................................................................
3
SUMMARY PRODUCT
INFORMATION......................................................................................
3
INDICATIONS AND CLINICAL USES
.........................................................................................
3
CONTRAINDICATIONS
.............................................................................................................
3
WARNINGS AND PRECAUTIONS
.............................................................................................
3
ADVERSE
REACTIONS.............................................................................................................
4
DRUG INTERACTIONS
.............................................................................................................
5
DOSAGE AND ADMINISTRATION
.............................................................................................
6
OVERDOSAGE..........................................................................................................................
6
ACTION AND CLINICAL PHARMACOLOGY
..............................................................................
6
STORAGE AND STABILITY
.......................................................................................................
7
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................................. 7
PART II: SCIENTIFIC INFORMATION
...........................................................................................
9
PHARMACEUTICAL INFORMATION
.............................................