RATIO-SALBUTAMOL SOLUTION

País: Canadà

Idioma: anglès

Font: Health Canada

ingredients actius:

SALBUTAMOL (SALBUTAMOL SULFATE)

Disponible des:

TEVA CANADA LIMITED

Codi ATC:

R03AC02

Designació comuna internacional (DCI):

SALBUTAMOL

Dosis:

2MG

formulario farmacéutico:

SOLUTION

Composición:

SALBUTAMOL (SALBUTAMOL SULFATE) 2MG

Vía de administración:

INHALATION

Unidades en paquete:

2.5ML

tipo de receta:

Prescription

Área terapéutica:

SELECTIVE BETA 2-ADRENERGIC AGONISTS

Resumen del producto:

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

Estat d'Autorització:

CANCELLED POST MARKET

Data d'autorització:

2018-06-22

Fitxa tècnica

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
.............................................................................................................
3
INDICATIONS AND CLINICAL USE
....................................................................................................................
3
CONTRAINDICATIONS
.........................................................................................................................................
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
.................................................