連續攜帶型腹膜透析液１．５％，１３０ＭＭＯＬ　ＮＡ＋

Land: Taiwan

Språk: kinesisk

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

Aktiv ingrediens:

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

Tilgjengelig fra:

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)

Legemiddelform:

透析用液劑

Sammensetning:

SODIUM LACTATE (4008000900) 3.93MG; CALCIUM CHLORIDE DIHYDRATE (4012000350) 0.294MG; SODIUM CHLORIDE (4012002100) 5.553MG; DEXTROSE (4020000500) 1.5%; DEXTROSE MONOHYDRATE (4020000570) 16.5MG; 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) 0.050MG

Enheter i pakken:

袋裝

Klasse:

製　劑

Resept typen:

限由醫師使用

Produsert av:

LABORATORIUM DR. G. BICHSEL AG WEISSENAUSTRASSE 3800 UNTERSEEN CH

Indikasjoner:

腎功能衰竭病患用以透析血中毒素

Produkt oppsummering:

註銷日期: 2005/06/15; 註銷理由: 未展延而逾期者; 有效日期: 1993/06/23; 英文品名: PERITONEAL DIALYSIS SOLUTION CAPD 1.5%, 130MMOL NA(+)

Autorisasjon status:

已註銷

Autorisasjon dato:

1988-06-23