MOGADON TABLET

Land: Canada

Taal: Engels

Bron: Health Canada

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Download Productkenmerken (SPC)
12-08-2021

Werkstoffen:

NITRAZEPAM

Beschikbaar vanaf:

AA PHARMA INC

ATC-code:

N05CD02

INN (Algemene Internationale Benaming):

NITRAZEPAM

Dosering:

5MG

farmaceutische vorm:

TABLET

Samenstelling:

NITRAZEPAM 5MG

Toedieningsweg:

ORAL

Eenheden in pakket:

100

Prescription-type:

Targeted (CDSA IV)

Therapeutisch gebied:

BENZODIAZEPINES

Product samenvatting:

Active ingredient group (AIG) number: 0114345001; AHFS:

Autorisatie-status:

APPROVED

Autorisatie datum:

2013-09-16

Productkenmerken

                                Page 1 of 27
PRODUCT MONOGRAPH
MOGADON
®
Nitrazepam Tablets BP
5 mg, 10 mg
Hypnotic and Anticonvulsant
AA PHARMA INC.
DATE OF REVISION:
1156 Creditstone Road, Unit#1
August 12, 2021
Vaughan, Ontario
L4K 4N7
Control No: 248565
Page 2 of 27
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.................................................... 3
SUMMARY PRODUCT
INFORMATION.........................................................................
3
INDICATIONS AND CLINICAL USE
..............................................................................
3
CONTRAINDICATIONS
..................................................................................................
3
WARNINGS AND
PRECAUTIONS..................................................................................
4
ADVERSE REACTIONS
.................................................................................................10
POST-MARKET ADVERSE REACTIONS
......................................................................10
DRUG INTERACTIONS
..................................................................................................11
SERIOUS DRUG INTERACTIONS
.................................................................................11
DOSAGE AND ADMINISTRATION
...............................................................................11
DOSING CONSIDERATIONS
.........................................................................................11
OVERDOSAGE
...............................................................................................................13
ACTION AND CLINICAL PHARMACOLOGY
..............................................................13
STORAGE AND STABILITY
..........................................................................................15
DOSAGE FORMS, COMPOSITION AND PACKAGING
................................................15
PART II: SCIENTIFIC INFORMATION
.........................................................................
16
PHARMACEUTICAL INFORMATION
.................
                                
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