ALLEGRA 12 HOUR TABLET

Country: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

FEXOFENADINE HYDROCHLORIDE

Disponibbli minn:

SANOFI CONSUMER HEALTH INC

Kodiċi ATC:

R06AX26

INN (Isem Internazzjonali):

FEXOFENADINE

Dożaġġ:

60MG

Għamla farmaċewtika:

TABLET

Kompożizzjoni:

FEXOFENADINE HYDROCHLORIDE 60MG

Rotta amministrattiva:

ORAL

Unitajiet fil-pakkett:

15G/50G

Tip ta 'preskrizzjoni:

OTC

Żona terapewtika:

SECOND GENERATION ANTIHISTAMINES

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0131730001; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2000-06-02

Karatteristiċi tal-prodott

                                _ALLEGRA_
_®_
_ 12 Hour (fexofenadine hydrochloride) _
_ALLEGRA_
_®_
_ 24 Hour (fexofenadine hydrochloride) _
_ALLEGRA_
_®_
_ HIVES (fexofenadine hydrochloride) _
_Page 1 of 35 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
ALLEGRA
® 12 HOUR
Fexofenadine hydrochloride tablets
Tablets, 60 mg, Oral
Manufacturer’s Standard ALLEGRA
® 24 HOUR
Fexofenadine hydrochloride tablets
Tablets, 120 mg, Oral
Manufacturer’s Standard
ALLEGRA
® HIVES
Fexofenadine hydrochloride tablets
Tablets, 60 mg, Oral
Manufacturer’s Standard
Histamine H
1
Receptor Antagonist
Sanofi Consumer Health Inc.
2905 Place Louis-R. Renaud
Laval, QC H7V 0A3
Date of Revision:
October 5, 2021
Submission
Control Number: 252314
_ _
_ALLEGRA_
_®_
_ 12 Hour (fexofenadine hydrochloride) _
_ALLEGRA_
_®_
_ 24 Hour (fexofenadine hydrochloride) _
_ALLEGRA_
_®_
_ HIVES (fexofenadine hydrochloride) _
_Page 2 of 35_
RECENT MAJOR LABEL CHANGES
Patient Medication Information
04/2021
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 ............................................................................
5
4.1 Dosing Considerations
........................
                                
                                Aqra d-dokument sħiħ
                                
                            

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