APO-DIPYRIDAMOLE TABLET

Land: Kanada

Sprache: Englisch

Quelle: Health Canada

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Fachinformation Fachinformation (SPC)
10-08-2021

Wirkstoff:

DIPYRIDAMOLE

Verfügbar ab:

APOTEX INC

ATC-Code:

B01AC07

INN (Internationale Bezeichnung):

DIPYRIDAMOLE

Dosierung:

75MG

Darreichungsform:

TABLET

Zusammensetzung:

DIPYRIDAMOLE 75MG

Verabreichungsweg:

ORAL

Einheiten im Paket:

250ML

Verschreibungstyp:

Prescription

Therapiebereich:

MISCELLANEOUS VASODILATATING AGENTS

Produktbesonderheiten:

Active ingredient group (AIG) number: 0106621003; AHFS:

Berechtigungsstatus:

APPROVED

Berechtigungsdatum:

2021-08-12

Fachinformation

                                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
.............................................
                                
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Fachinformation Fachinformation Französisch 10-08-2021

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