APO-DIPYRIDAMOLE TABLET

Land: Canada

Sprog: engelsk

Kilde: Health Canada

Køb det nu

Produktets egenskaber Produktets egenskaber (SPC)
10-08-2021

Aktiv bestanddel:

DIPYRIDAMOLE

Tilgængelig fra:

APOTEX INC

ATC-kode:

B01AC07

INN (International Name):

DIPYRIDAMOLE

Dosering:

50MG

Lægemiddelform:

TABLET

Sammensætning:

DIPYRIDAMOLE 50MG

Indgivelsesvej:

ORAL

Enheder i pakken:

250ML

Recept type:

Prescription

Terapeutisk område:

MISCELLANEOUS VASODILATATING AGENTS

Produkt oversigt:

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

Autorisation status:

APPROVED

Autorisation dato:

2021-08-12

Produktets egenskaber

                                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
.............................................
                                
                                Læs hele dokumentet
                                
                            

Dokumenter på andre sprog

Produktets egenskaber Produktets egenskaber fransk 10-08-2021

Søg underretninger relateret til dette produkt