TRAMAPHEN-ODAN TABLET

Страна: Канада

Език: английски

Източник: Health Canada

Купи го сега

Активна съставка:

ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE

Предлага се от:

ODAN LABORATORIES LTD

АТС код:

N02AJ13

INN (Международно Name):

TRAMADOL AND PARACETAMOL

дозиране:

325MG; 37.5MG

Лекарствена форма:

TABLET

Композиция:

ACETAMINOPHEN 325MG; TRAMADOL HYDROCHLORIDE 37.5MG

Начин на приложение:

ORAL

Броя в опаковка:

100/500

Вид предписание :

Narcotic (CDSA I)

Терапевтична област:

OPIATE AGONISTS

Каталог на резюме:

Active ingredient group (AIG) number: 0250601001; AHFS:

Статус Оторизация:

CANCELLED POST MARKET

Дата Оторизация:

2014-10-31

Данни за продукта

                                1 | P a g e
PRODUCT MONOGRAPH
PR
TRAMAPHEN-ODAN
Acetaminophen and Tramadol hydrochloride tablets, House Std
37.5 mg tramadol hydrochloride/325 mg acetaminophen
Centrally Acting Analgesic
ODAN LABORATORIES LTD.
DATE OF PREPARATION:
325 STILLVIEW AVENUE
JULY 3, 2012
POINTE-CLAIRE, QC
CANADA H9R 2Y6
Control# 156402
2 | P a g e
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
..............................................................................
3
SUMMARY PRODUCT INFORMATION
..........................................................................................
3
INDICATIONS AND CLINICAL USE
.................................................................................................
3
CONTRAINDICATIONS
..................................................................................................................
4
WARNINGS AND PRECAUTIONS
...................................................................................................
4
ADVERSE REACTIONS
...................................................................................................................
9
DRUG ABUSE, ADDICTION AND DEPENDENCE
...........................................................................
12
DRUG INTERACTIONS
.................................................................................................................
13
DOSAGE AND ADMINISTRATION
...............................................................................................
14
OVERDOSAGE
.............................................................................................................................
15
ACTION AND CLINICAL PHARMACOLOGY
..................................................................................
17
STORAGE AND STABILITY
...........................................................................................................
21
DOSAGE FORMS, COMPOSITION AND PACKAGING
................................................................... 21
PART II: SCIENTIFIC INFORMATION
........................
                                
                                Прочетете целия документ
                                
                            

Документи на други езици

Данни за продукта Данни за продукта френски 03-07-2012

Сигнали за търсене, свързани с този продукт

Преглед на историята на документите