IPG-CETIRIZINE TABLET

Land: Canada

Sprog: engelsk

Kilde: Health Canada

Køb det nu

Hent Produktets egenskaber (SPC)
24-01-2023

Aktiv bestanddel:

CETIRIZINE HYDROCHLORIDE

Tilgængelig fra:

MARCAN PHARMACEUTICALS INC

ATC-kode:

R06AE07

INN (International Name):

CETIRIZINE

Dosering:

5MG

Lægemiddelform:

TABLET

Sammensætning:

CETIRIZINE HYDROCHLORIDE 5MG

Indgivelsesvej:

ORAL

Enheder i pakken:

30/100/500

Recept type:

OTC

Terapeutisk område:

SECOND GENERATION ANTIHISTAMINES

Produkt oversigt:

Active ingredient group (AIG) number: 0122686002; AHFS:

Autorisation status:

APPROVED

Autorisation dato:

2016-06-29

Produktets egenskaber

                                IPG-CETIRIZINE - Product Monograph
Page 1 of 34
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
IPG-CETIRIZINE
Cetirizine Hydrochloride Tablets
Tablets, 5 mg, 10 mg, Oral
Histamine H
1
Receptor Antagonist
Marcan Pharmaceuticals Inc.
2 Gurdwara Road, Suite #112
Ottawa, ON, K2E 1A2
Date of Initial Authorization:
JUN 06, 2014
Date of Revision:
JAN 24, 2023
Submission Control Number: 267528
IPG-CETIRIZINE - Product Monograph
Page 2 of 34
RECENT MAJOR LABEL CHANGES
N/A
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED
.
RECENT MAJOR LABEL CHANGES
.............................................................................................2
TABLE OF CONTENTS
...............................................................................................................2
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................4
1
INDICATIONS
...............................................................................................................4
1.1
Pediatrics
...........................................................................................................4
1.2
Geriatrics............................................................................................................4
2
CONTRAINDICATIONS
..................................................................................................4
4
DOSAGE AND ADMINISTRATION
..................................................................................4
4.1
Dosing
Considerations.........................................................................................4
4.2
Recommended Dose and Dosage
Adjustment......................................................4
4.4
Administration....................................................................................................5
4.5
Missed Dose
.......................................................................................................5
5
OVERDOSAGE
...............
                                
                                Læs hele dokumentet
                                
                            

Dokumenter på andre sprog

Produktets egenskaber Produktets egenskaber fransk 24-01-2023

Søg underretninger relateret til dette produkt