PRO-ENALAPRIL - 5 TABLET

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

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Aktivní složka:

ENALAPRIL MALEATE

Dostupné s:

PRO DOC LIMITEE

ATC kód:

C09AA02

INN (Mezinárodní Name):

ENALAPRIL

Dávkování:

5MG

Léková forma:

TABLET

Složení:

ENALAPRIL MALEATE 5MG

Podání:

ORAL

Jednotky v balení:

100/500

Druh předpisu:

Prescription

Terapeutické oblasti:

ANGIOTENSIN-CONVERTING ENZYME INHIBITORS

Přehled produktů:

Active ingredient group (AIG) number: 0117649003; AHFS:

Stav Autorizace:

APPROVED

Datum autorizace:

2008-06-13

Charakteristika produktu

                                _PRO-ENALAPRIL (Enalapril Maleate Tablets_)
_Page 1 of 49_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
PRO-ENALAPRIL – 2.5,
PR
PRO-ENALAPRIL – 5, PR
PRO-ENALAPRIL – 10, PR
PRO-ENALAPRIL – 20
Enalapril Maleate Tablets
Tablets 2.5 mg, 5 mg, 10 mg, and 20 mg, oral
USP
Angiotensin Converting Enzyme Inhibitor
PRO DOC LTÉE.
2925 Boulevard Industriel
Laval, Quebec
H7L 3W9
Submission Control Number: 277145
Date of Initial Authorization:
JUN 13, 2008
Date
of Revision:
AUG 09, 2023
_PRO-ENALAPRIL (Enalapril Maleate Tablets_)
_Page 2 of 49_
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS
08/2023
4 DOSAGE AND ADMINISTRATION
08/2023
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
............................................................................................
2
TABLE OF CONTENTS
..............................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................................
4
1
INDICATIONS
.............................................................................................................
4
1.1 Pediatrics
.................................................................................................................
4
1.2 Geriatrics
.................................................................................................................
4
2
CONTRAINDICATIONS
...............................................................................................
4
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
.......................................................... 5
4
DOSAGE AND ADMINISTRATION
...............................................................................
5
4.1 Dosing Considerations
.............................................................................................
5
4.2 Recommended Dose and Dosage Adjustment
.............................
                                
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