CLARITIN ALLERGY + SINUS TABLET (IMMEDIATE AND EXTENDED RELEASE)

Country: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ingredjent attiv:

PSEUDOEPHEDRINE SULFATE; LORATADINE

Disponibbli minn:

BAYER INC

Kodiċi ATC:

R01BA52

INN (Isem Internazzjonali):

PSEUDOEPHEDRINE, COMBINATIONS

Dożaġġ:

120MG; 5MG

Għamla farmaċewtika:

TABLET (IMMEDIATE AND EXTENDED RELEASE)

Kompożizzjoni:

PSEUDOEPHEDRINE SULFATE 120MG; LORATADINE 5MG

Rotta amministrattiva:

ORAL

Unitajiet fil-pakkett:

10/20/30

Tip ta 'preskrizzjoni:

OTC

Żona terapewtika:

SECOND GENERATION ANTIHISTAMINES

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0245861002; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2014-12-08

Karatteristiċi tal-prodott

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PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
CLARITIN® ALLERGY + SINUS
Loratadine and Pseudoephedrine Sulfate
Modified-Release Tablets, Professed Standard
5 mg Loratadine and 120 mg Pseudoephedrine Sulfate; Oral
CLARITIN® ALLERGY + SINUS EXTRA STRENGTH
Loratadine and Pseudoephedrine Sulfate
Modified-Release Tablets, Professed Standard
10 mg Loratadine and 240 mg Pseudoephedrine Sulfate; Oral
Histamine H1 receptor antagonist/Sympathomimetic amine
Bayer Inc.
2920 Matheson Blvd. E
Mississauga, ON
L4W 5R6
Date of Initial Authorization:
Claritin® Allergy + Sinus:
2-Mar-1993
Claritin® Allergy +Sinus Extra
Strength:
4-Dec-2004
Date of Revision:
NOV-01-2022
Submission Control Number: 265671
® TM see www.bayer.ca/tm-mc
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TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED
.
TABLE OF CONTENTS
...........................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
.................................................................. 4
1.
INDICATIONS................................................................................................................
4
1.1
Pediatrics
..................................................................................................................
4
1.2
Geriatrics...................................................................................................................
4
2.
CONTRAINDICATIONS
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4
4.
DOSAGE AND ADMI