APO-ACEBUTOLOL TABLET

Land: Canada

Taal: Engels

Bron: Health Canada

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24-10-2018

Werkstoffen:

ACEBUTOLOL (ACEBUTOLOL HYDROCHLORIDE)

Beschikbaar vanaf:

APOTEX INC

ATC-code:

C07AB04

INN (Algemene Internationale Benaming):

ACEBUTOLOL

Dosering:

100MG

farmaceutische vorm:

TABLET

Samenstelling:

ACEBUTOLOL (ACEBUTOLOL HYDROCHLORIDE) 100MG

Toedieningsweg:

ORAL

Eenheden in pakket:

100 & 500 TABLETS

Prescription-type:

Prescription

Therapeutisch gebied:

BETA-ADRENERGIC BLOCKING AGENTS

Product samenvatting:

Active ingredient group (AIG) number: 0131282001; AHFS:

Autorisatie-status:

MARKETED

Autorisatie datum:

1995-12-31

Productkenmerken

                                _APO-ACEBUTOLOL Product Monograph _
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_Page 1 of 34 _
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PRODUCT MONOGRAPH
PR APO-ACEBUTOLOL
ACEBUTOLOL TABLETS (AS ACEBUTOLOL HYDROCHLORIDE)
APOTEX STANDARD
100 MG, 200 MG AND 400 MG TABLETS
ANTIHYPERTENSIVE AND ANTI-ANGINAL AGENT
APOTEX INC.
DATE OF REVISION:
150 SIGNET DRIVE
OCTOBER 24, 2018
TORONTO, ONTARIO
M9L 1T9
CONTROL NUMBER# 220342
_APO-ACEBUTOLOL Product Monograph _
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_Page 2 of 34 _
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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
..............................................................................................................................................
9
DRUG INTERACTIONS
.............................................................................................................................................
11
DOSAGE AND ADMINISTRATION
.........................................................................................................................
15
OVERDOSAGE
...........................................................................................................................................................
16
ACTION AND CLINICAL PHARMACOLOGY
.......................................................................................................
17
STORAGE AND STABILITY
...........................................
                                
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