MYLAN-IRBESARTAN HCTZ TABLET

Country: Канада

Језик: Енглески

Извор: Health Canada

Активни састојак:

IRBESARTAN; HYDROCHLOROTHIAZIDE

Доступно од:

MYLAN PHARMACEUTICALS ULC

АТЦ код:

C09DA04

INN (Међународно име):

IRBESARTAN AND DIURETICS

Дозирање:

300MG; 25MG

Фармацеутски облик:

TABLET

Састав:

IRBESARTAN 300MG; HYDROCHLOROTHIAZIDE 25MG

Пут администрације:

ORAL

Јединице у пакету:

90

Тип рецептора:

Prescription

Терапеутска област:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Резиме производа:

Active ingredient group (AIG) number: 0240086003; AHFS:

Статус ауторизације:

CANCELLED PRE MARKET

Датум одобрења:

2016-11-02

Карактеристике производа

1
PRODUCT MONOGRAPH
PR MYLAN-IRBESARTAN HCTZ
Irbesartan and Hydrochlorothiazide Tablets
150/12.5 mg, 300/12.5 mg and 300/25 mg
Manufacturer’s Standard
Angiotensin II AT
1
Receptor Blocker / Diuretic
Mylan Pharmaceuticals ULC
85 Advance Road
Etobicoke, ON
M8Z 2S6
Submission Control No.: 189365
Date of Revision: November 24, 2015
2
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
...........................................................................................................
9
DRUG INTERACTIONS
.........................................................................................................
14
DOSAGE AND ADMINISTRATION
.....................................................................................
20
OVERDOSAGE
.......................................................................................................................
22
ACTION AND CLINICAL PHARMACOLOGY
................................................................... 22
STORAGE AND STABILITY
.................................................................................................
26
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................... 26
PART II: SCIENTIFIC INFORMATION
...............................................................................
27
PHARMACEUTICAL INFORMATION
.................................................................................
27
CLINICAL TRIALS
.......................................................