RATIO-SALBUTAMOL SOLUTION

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Aktiivinen ainesosa:

SALBUTAMOL (SALBUTAMOL SULFATE)

Saatavilla:

TEVA CANADA LIMITED

ATC-koodi:

R03AC02

INN (Kansainvälinen yleisnimi):

SALBUTAMOL

Annos:

2MG

Lääkemuoto:

SOLUTION

Koostumus:

SALBUTAMOL (SALBUTAMOL SULFATE) 2MG

Antoreitti:

INHALATION

Kpl paketissa:

2.5ML

Prescription tyyppi:

Prescription

Terapeuttinen alue:

SELECTIVE BETA 2-ADRENERGIC AGONISTS

Tuoteyhteenveto:

Active ingredient group (AIG) number: 0108887001; AHFS:

Valtuutuksen tilan:

CANCELLED POST MARKET

Valtuutus päivämäärä:

2018-06-22

Valmisteyhteenveto

PRODUCT MONOGRAPH
RATIO-SALBUTAMOL
salbutamol sulphate nebules P.F. 1.25MG/2.5 ML, 5.0 MG/2.5 ML AMPOULES
Bronchodilator
(beta
2
-adrenergic stimulant)
TEVA CANADA LIMITED..
30 NOVOPHARM COURT
TORONTO, ONTARIO
CANADA, M1B 2K9
Control: 165512
DATE OF PREPARATION:
JULY 3, 2013
Teva Canada Limited.
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TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
..........................................................................................
3
SUMMARY PRODUCT INFORMATION
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3
INDICATIONS AND CLINICAL USE
....................................................................................................................
3
CONTRAINDICATIONS
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3
WARNINGS AND PRECAUTIONS
......................................................................................................................
3
ADVERSE REACTIONS
........................................................................................................................................
7
DRUG INTERACTIONS
.........................................................................................................................................
7
DOSAGE AND ADMINISTRATION
....................................................................................................................
10
OVERDOSAGE
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11
ACTION AND CLINICAL PHARMACOLOGY
...................................................................................................
12
STORAGE AND STABILITY
...............................................................................................................................
13
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................