ROPINIROLE TABLET

国家: 加拿大

语言: 英文

来源: Health Canada

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下载 产品特点 (SPC)
10-02-2021

有效成分:

ROPINIROLE (ROPINIROLE HYDROCHLORIDE)

可用日期:

SANIS HEALTH INC

ATC代码:

N04BC04

INN(国际名称):

ROPINIROLE

剂量:

0.25MG

药物剂型:

TABLET

组成:

ROPINIROLE (ROPINIROLE HYDROCHLORIDE) 0.25MG

给药途径:

ORAL

每包单位数:

100

处方类型:

Prescription

治疗领域:

NONERGOT-DERIVATIVE DOPAMINE RECEPTOR AGONISTS

產品總結:

Active ingredient group (AIG) number: 0132618001; AHFS:

授权状态:

APPROVED

授权日期:

2010-06-18

产品特点

                                _ _
_ROPINIROLE 0.25 mg, 1 mg, Tablets _
_Page 1 of 53_
PRODUCT MONOGRAPH
Pr
ROPINIROLE
Ropinirole Tablets, USP
0.25 mg and 1 mg ropinirole (as ropinirole hydrochloride)
Antiparkinsonian Agent / Dopamine Agonist
Sanis Health Inc.
1 President’s Choice Circle
Brampton, Ontario
L6Y 5S5
Date of Revision:
February 10, 2021
Submission Control No.: 244016
_ _
_ROPINIROLE 0.25 mg, 1 mg Tablets _
_Page 2 of 53_
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
.................................................................................................
21
DOSAGE AND ADMINISTRATION
.............................................................................
23
OVERDOSAGE
...............................................................................................................
24
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 25
STORAGE AND STABILITY
.........................................................................................
29
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 29
PART II: SCIENTIFIC INFORMATION
..............................................................................
30
PHARMACEUTICAL INFORMATION
.........................................................................
30
CLINICAL TRIALS
...............................................................................
                                
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