RANITIDINE TABLET

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktivní složka:

RANITIDINE (RANITIDINE HYDROCHLORIDE)

Dostupné s:

PRO DOC LIMITEE

ATC kód:

A02BA02

INN (Mezinárodní Name):

RANITIDINE

Dávkování:

150MG

Léková forma:

TABLET

Složení:

RANITIDINE (RANITIDINE HYDROCHLORIDE) 150MG

Podání:

ORAL

Jednotky v balení:

100/500/60

Druh předpisu:

Prescription

Terapeutické oblasti:

HISTAMINE H2-ANTAGONISTS

Přehled produktů:

Active ingredient group (AIG) number: 0115150002; AHFS:

Stav Autorizace:

CANCELLED POST MARKET

Datum autorizace:

2023-07-10

Charakteristika produktu

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RANITIDINE_ _
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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_ _
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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
................