ALLERTIN CAPSULE

Ülke: Kanada

Dil: İngilizce

Kaynak: Health Canada

şimdi satın al

Indir Ürün özellikleri (SPC)
25-09-2019

Aktif bileşen:

LORATADINE

Mevcut itibaren:

APOTEX INC

ATC kodu:

R06AX13

INN (International Adı):

LORATADINE

Doz:

10MG

Farmasötik formu:

CAPSULE

Kompozisyon:

LORATADINE 10MG

Uygulama yolu:

ORAL

Paketteki üniteler:

12/24

Reçete türü:

OTC

Terapötik alanı:

SECOND GENERATION ANTIHISTAMINES

Ürün özeti:

Active ingredient group (AIG) number: 0120416001; AHFS:

Yetkilendirme durumu:

APPROVED

Yetkilendirme tarihi:

2012-08-02

Ürün özellikleri

                                Page 2 of 20
PRODUCT MONOGRAPH
ALLERTIN
LORATADINE CAPSULES, 10 MG
HISTAMINE H
1 RECEPTOR ANTAGONIST
APOTEX INC.
DATE OF REVISION:
150 SIGNET DRIVE
SEPTEMBER 25, 2019
TORONTO, ONTARIO
CANADA M9L 1T9
CONTROL #: 231181
Page 3 of 20
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................
4
SUMMARY PRODUCT INFORMATION
.............................................................................................
4
INDICATIONS AND CLINICAL USE
...................................................................................................
4
CONTRAINDICATIONS
........................................................................................................................
4
WARNINGS AND PRECAUTIONS
.......................................................................................................
4
ADVERSE REACTIONS
.........................................................................................................................
5
DRUG INTERACTIONS
.........................................................................................................................
6
DOSAGE AND ADMINISTRATION
.....................................................................................................
7
OVERDOSAGE
.......................................................................................................................................
7
ACTION AND CLINICAL
PHARMACOLOGY....................................................................................
8
STORAGE AND STABILITY
.................................................................................................................
9
SPECIAL HANDLING INSTRUCTIONS
..............................................................................................
9
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................................... 9
PART II: SCIENTIFIC INFORMATION
.....................................................................
                                
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