TEVA-SALBUTAMOL HFA METERED-DOSE AEROSOL

国家: 加拿大

语言: 英文

来源: Health Canada

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20-03-2018

有效成分:

SALBUTAMOL (SALBUTAMOL SULFATE)

可用日期:

TEVA CANADA LIMITED

ATC代码:

R03AC02

INN(国际名称):

SALBUTAMOL

剂量:

100MCG

药物剂型:

METERED-DOSE AEROSOL

组成:

SALBUTAMOL (SALBUTAMOL SULFATE) 100MCG

给药途径:

INHALATION

每包单位数:

200 DOSES

处方类型:

Prescription

治疗领域:

SELECTIVE BETA 2-ADRENERGIC AGONISTS

產品總結:

Active ingredient group (AIG) number: 0108887013; AHFS:

授权状态:

APPROVED

授权日期:

2009-12-07

产品特点

                                _Page 1_
PRODUCT MONOGRAPH
Pr
TEVA-SALBUTAMOL HFA
salbutamol (as salbutamol sulfate)
Inhalation Aerosol
100 mcg salbutamol per actuation
Bronchodilator
(beta
2
-adrenergic agonist)
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
M1B 2K9
www.tevacanada.com
Submission Control No: 213098
Date of Revision:
March 20, 2018
_Page 2_
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
....................................................................................................
7
DRUG INTERACTIONS
..................................................................................................
10
DOSAGE AND ADMINISTRATION
..............................................................................
11
OVERDOSAGE
.................................................................................................................
12
ACTION AND CLINICAL PHARMACOLOGY
............................................................. 13
STORAGE AND STABILITY
..........................................................................................
15
SPECIAL HANDLING INSTRUCTIONS
........................................................................
15
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................. 15
PART II: SCIENTIFIC INFORMATION
...............................................................................
16
PHARMACEUTICAL INFORMATION
..........................................................................
16
CLINICAL TRIALS
..........................
                                
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