RANITIDINE TABLET

Страна: Канада

Език: английски

Източник: Health Canada

Активна съставка:

RANITIDINE (RANITIDINE HYDROCHLORIDE)

Предлага се от:

PRO DOC LIMITEE

АТС код:

A02BA02

INN (Международно Name):

RANITIDINE

дозиране:

300MG

Лекарствена форма:

TABLET

Композиция:

RANITIDINE (RANITIDINE HYDROCHLORIDE) 300MG

Начин на приложение:

ORAL

Броя в опаковка:

100/30

Вид предписание :

Prescription

Терапевтична област:

HISTAMINE H2-ANTAGONISTS

Каталог на резюме:

Active ingredient group (AIG) number: 0115150001; AHFS:

Статус Оторизация:

CANCELLED POST MARKET

Дата Оторизация:

2023-07-10

Данни за продукта

_ _
RANITIDINE_ _
_Page 1 of 28_
PRODUCT MONOGRAPH
PR RANITIDINE
Ranitidine Tablets, USP
150 mg & 300 mg ranitidine (as ranitidine hydrochloride)
Histamine H
2
-receptor antagonist
PRO DOC LTÉE
2925, boul. Industriel
Laval, Quebec
H7L 3W9
Date of Revision:
September 18, 2019
Submission Control No: 229390
RANITIDINE_ _
_Page 2 of 28_
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
....................................................................................................6
DRUG INTERACTIONS
....................................................................................................7
DOSAGE AND ADMINISTRATION
................................................................................8
OVERDOSAGE
................................................................................................................10
ACTION AND CLINICAL PHARMACOLOGY
............................................................10
STORAGE AND STABILITY
..........................................................................................12
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................12
PART II: SCIENTIFIC INFORMATION
................................................................................13
PHARMACEUTICAL INFORMATION
..........................................................................13
CLINICAL TRIALS
..........................................................................................................14
DETAILED PHARMACOLOGY
................