MAR-DONEPEZIL TABLET

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

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Aktivní složka:

DONEPEZIL HYDROCHLORIDE

Dostupné s:

MARCAN PHARMACEUTICALS INC

ATC kód:

N06DA02

INN (Mezinárodní Name):

DONEPEZIL

Dávkování:

10MG

Léková forma:

TABLET

Složení:

DONEPEZIL HYDROCHLORIDE 10MG

Podání:

ORAL

Jednotky v balení:

100/500

Druh předpisu:

Prescription

Terapeutické oblasti:

PARASYMPATHOMEMETIC (CHOLINERGIC) AGENTS

Přehled produktů:

Active ingredient group (AIG) number: 0131548002; AHFS:

Stav Autorizace:

APPROVED

Datum autorizace:

2013-12-27

Charakteristika produktu

                                Page 1 of 50
PRODUCT MONOGRAPH
Pr
MAR-DONEPEZIL
Donepezil Hydrochloride Tablets, House Std
5 and 10 mg
CHOLINESTERASE INHIBITOR
Marcan Pharmaceuticals Inc. Date of Revision:
2 Gurdwara Road, Suite 112
February 10, 2020
Ottawa, Ontario
K2E 1A2
Submission Control No.: 235582
Page 2 of 50
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
.......................................................................
3
INDICATIONS AND CLINICAL USE
.............................................................................
3
CONTRAINDICATIONS
..................................................................................................
3
WARNINGS AND PRECAUTIONS
.................................................................................
3
ADVERSE REACTIONS
...................................................................................................
7
DRUG INTERACTIONS
.................................................................................................
16
DOSAGE AND ADMINISTRATION
.............................................................................
17
OVERDOSAGE
...............................................................................................................
18
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 18
STORAGE AND STABILITY
.........................................................................................
21
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 21
PART II: SCIENTIFIC INFORMATION
...............................................................................
22
PHARMACEUTICAL INFORMATION
.........................................................................
22
CLINICAL TRIALS
.........................................................................................................
24
DETAILED PHARMACOLOGY
...................................................................
                                
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