SANDOZ ESCITALOPRAM TABLET

দেশ: কানাডা

ভাষা: ইংরেজি

সূত্র: Health Canada

সক্রিয় উপাদান:

ESCITALOPRAM (ESCITALOPRAM OXALATE)

থেকে পাওয়া:

SANDOZ CANADA INCORPORATED

এটিসি কোড:

N06AB10

INN (আন্তর্জাতিক নাম):

ESCITALOPRAM

ডোজ:

10MG

ফার্মাসিউটিকাল ফর্ম:

TABLET

রচনা:

ESCITALOPRAM (ESCITALOPRAM OXALATE) 10MG

প্রশাসন রুট:

ORAL

প্যাকেজ ইউনিট:

30/100

প্রেসক্রিপশন টাইপ:

Prescription

থেরাপিউটিক এলাকা:

SELECTIVE-SEROTONIN REUPTAKE INHIBITORS

পণ্য সারাংশ:

Active ingredient group (AIG) number: 0150435002; AHFS:

অনুমোদন অবস্থা:

APPROVED

অনুমোদন তারিখ:

2014-09-10

পণ্য বৈশিষ্ট্য

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_Sandoz Escitalopram _
_Page 1 of 61_
PRODUCT MONOGRAPH
PR SANDOZ ESCITALOPRAM
Escitalopram Oxalate Tablets
10, 20 mg as escitalopram
ANTIDEPRESSANT / ANXIOLYTIC / ANTIOBSESSIONAL
Sandoz Canada Inc.
Date of Revision: October 6, 2020
110 Rue de Lauzon
Boucherville, QC
J4B 1E6
Submission Control No: 240809
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_Sandoz Escitalopram _
_Page 2 of 61_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY
PRODUCT
INFORMATION
................................................................................
3
INDICATIONS
AND
CLINICAL
USE
.....................................................................................
3
CONTRAINDICATIONS
..........................................................................................................
4
WARNINGS
AND
PRECAUTIONS
.........................................................................................
5
ADVERSE
REACTIONS
.........................................................................................................
11
DRUG
INTERACTIONS
.........................................................................................................
27
DOSAGE
AND
ADMINISTRATION
.....................................................................................
33
OVERDOSAGE
.......................................................................................................................
35
ACTION
AND
CLINICAL
PHARMACOLOGY
....................................................................
36
STORAGE
AND
STABILITY
.................................................................................................
38
DOSAGE
FORMS,
COMPOSITION
AND
PACKAGING ..................................................... 38
PART II: SCIENTIFIC INFORMATION
...............................................................................
40
PHARMACEUTICAL
INFORMATION
.................................................................................
40
CLINICAL
TRIALS
...................................