BUSTAB TABLET

국가: 캐나다

언어: 영어

출처: Health Canada

지금 구매하세요

제품 특성 요약 제품 특성 요약 (SPC)
23-11-2005

유효 성분:

BUSPIRONE HYDROCHLORIDE

제공처:

VALEANT CANADA LP / VALEANT CANADA S.E.C.

ATC 코드:

N05BE01

INN (International Name):

BUSPIRONE

복용량:

5MG

약제 형태:

TABLET

구성:

BUSPIRONE HYDROCHLORIDE 5MG

관리 경로:

ORAL

패키지 단위:

100/500

처방전 유형:

Prescription

치료 영역:

MISCELLANEOUS ANXIOLYTICS SEDATIVES AND HYPNOTICS

제품 요약:

Active ingredient group (AIG) number: 0116263002; AHFS:

승인 상태:

CANCELLED POST MARKET

승인 날짜:

2014-07-30

제품 특성 요약

                                1
PRODUCT MONOGRAPH
Pr
BUSTAB
Buspirone Hydrochloride Tablets
5 mg & 10 mg
USP
Anxiolytic
Valeant Canada Limited
4787 Levy Street
Montréal, Québec
H4R 2P9
NC Control No. 098261
Date of Preparation:
November 2, 2005
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 . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . 14
SYMPTOMS AND TREATMENT OF OVERDOSAGE . . . . . . . . . . . . . . . . .
. . . . . . . 14
ACTION AND CLINICAL PHARMACOLOGY . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . 15
STORAGE AND STABILITY . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . 17
DOSAGE FORMS, COMPOSITION AND PACKAGING . . . . . . . . . . . . . . .
. . . . . . . 17
PART II: SCIENTIFIC INFORMATION . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . 18
PHARMACEUTICAL INFORMATION . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . 18
CLINICAL TRIALS . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . 19
DETAILED PHARMACOLOGY . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . 19
MICROBIOLOGY . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . 
                                
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