TEVA-DULOXETINE DR CAPSULE (DELAYED RELEASE)

Страна: Канада

Език: английски

Източник: Health Canada

Купи го сега

Активна съставка:

DULOXETINE (DULOXETINE HYDROCHLORIDE)

Предлага се от:

TEVA CANADA LIMITED

АТС код:

N06AX21

INN (Международно Name):

DULOXETINE

дозиране:

60MG

Лекарствена форма:

CAPSULE (DELAYED RELEASE)

Композиция:

DULOXETINE (DULOXETINE HYDROCHLORIDE) 60MG

Начин на приложение:

ORAL

Броя в опаковка:

30/100

Вид предписание :

Prescription

Терапевтична област:

SELECTIVE SEROTONIN AND NOREPINEPHRINE-REUPTAKE INHIBITORS

Каталог на резюме:

Active ingredient group (AIG) number: 0152350002; AHFS:

Статус Оторизация:

CANCELLED PRE MARKET

Дата Оторизация:

2021-07-29

Данни за продукта

                                _ _
_TEVA-DULOXETINE _
_Page 1 of 81_
PRODUCT MONOGRAPH
PR
TEVA-DULOXETINE
Duloxetine Delayed Release Capsules, Mfr. Std.
Duloxetine (as duloxetine hydrochloride)
30 mg and 60 mg
ANALGESIC/ANTIDEPRESSANT/ANXIOLYTIC
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
M1B 2K9
Date of Preparation:
August 21, 2019
Date of Revision:
August 29, 2019
Submission Control No: 230092
_ _
_TEVA-DULOXETINE _
_Page 2 of 81_
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
.................................................................................................
19
DRUG INTERACTIONS
.................................................................................................
37
DOSAGE AND ADMINISTRATION
.............................................................................
41
OVERDOSAGE
...............................................................................................................
44
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 45
STORAGE AND STABILITY
.........................................................................................
48
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 49
PART II: SCIENTIFIC INFORMATION
...............................................................................
50
PHARMACEUTICAL INFORMATION
.........................................................................
50
CLINICAL TRIALS
....................................................................
                                
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Данни за продукта Данни за продукта френски 29-08-2019

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