連續攜帶型腹膜透析液４．０％，１３０ＭＭＯＬ　ＮＡ（＋）

국가: 대만

언어: 중국어

출처: 衛生福利部食品藥物管理署 (Ministry of Health and Welfare, Food And Drug Administration)

유효 성분:

SODIUM CHLORIDE;;SODIUM LACTATE;;CALCIUM CHLORIDE DIHYDRATE;;MAGNESIUM CARBONATE HEXAHYDRATE;;DEXTROSE MONOHYDRATE;;SODIUM ION;;CALCIUM ION;;MAGNESIUM ION;;CHLORIDE ION;;DEXTROSE

제공처:

寶錕貿易股份有限公司 台北巿士林區德行東路２９８號１樓 (36546883)

약제 형태:

透析用液劑

구성:

SODIUM LACTATE (4008000900) (100%) 3.93MG; CALCIUM CHLORIDE DIHYDRATE (4012000350) 0.294MG; SODIUM CHLORIDE (4012002100) 5.553MG; DEXTROSE (4020000500) 4.0%; DEXTROSE MONOHYDRATE (4020000570) 46.2MG; CALCIUM ION (4026000410) 2M.MOL; CHLORIDE ION (4026000510) 99.5M.MOL; MAGNESIUM ION (4026001110) 0.25M.MOL; SODIUM ION (4026001710) 130M.MOL; MAGNESIUM CARBONATE HEXAHYDRATE (5604002450) 0.05MG

패키지 단위:

袋裝

수업:

製　劑

처방전 유형:

限由醫師使用

Manufactured by:

LABORATORIUM DR. G. BICHSEL AG WEISSENAUSTRASSE 3800 UNTERSEEN CH

치료 징후:

腎功能衰竭病患用以透析血中毒素

제품 요약:

註銷日期: 2005/06/15; 註銷理由: 未展延而逾期者; 有效日期: 1993/06/22; 英文品名: PERITONEAL DIALYSIS SOLUTION CAPD 4.0%, 130MMOL NA(+)

승인 상태:

已註銷

승인 날짜:

1988-06-22