TFDA 藥品許可證

"費森尤斯" 均衡腹膜透析液2.3%葡萄糖,1.75MMOL/L鈣

Balance 2.3% glucose, 1.75 mmol/L calcium, solution for peritoneal dialysis

有效

基本資料

許可證字號: 衛署藥輸字第023907號
許可證種類: 製　劑
劑型: 透析用液劑
藥品類別: 限由醫師使用
管制藥品級別: —
法規處分狀態: 未註銷
效期狀態: 效期內
狀態基準日: 2026-08-16
發證日期: 2004-01-09
有效期限: 2029-01-09
異動日期: 2023-08-24

詳細處方成分

EACH ML OF SOLUTION A CONTAINS：SODIUM CHLORIDE4012002100 ↗11.279000 MG

EACH ML OF SOLUTION A CONTAINS：CALCIUM CHLORIDE DIHYDRATE4012000350 ↗0.515000 MG

EACH ML OF SOLUTION A CONTAINS：GLUCOSE MONOHYDRATE4020000760 ↗50.000000 MG

EACH ML OF SOLUTION A CONTAINS：MAGNESIUM CHLORIDE HEXAHYDRATE (EQ TO MAGNESIUM CHLORIDE 6H2O)4012001550 ↗0.203000 MG

EACH ML OF SOLUTION B CONTAINS：SODIUM S-LACTATE SOLUTION 50%4008000982 ↗15.690000 MG

EACH ML OF MIXED SOLUTION CONTAINS：SODIUM CHLORIDE4012002100 ↗5.640000 MG

EACH ML OF MIXED SOLUTION CONTAINS：SODIUM LACTATE4008000900 ↗3.925000 MG

EACH ML OF MIXED SOLUTION CONTAINS：CALCIUM CHLORIDE DIHYDRATE4012000350 ↗0.257000 MG

EACH ML OF MIXED SOLUTION CONTAINS：MAGNESIUM CHLORIDE HEXAHYDRATE (EQ TO MAGNESIUM CHLORIDE 6H2O)4012001550 ↗0.102000 MG

EACH ML OF MIXED SOLUTION CONTAINS：GLUCOSE MONOHYDRATE4020000760 ↗25.000000 MG

成分、含量及單位均保留官方列順序與原文；空值不推定。來源：藥品詳細處方成分資料集 · SHA bff64d27967b…

主成分略述（藥證原欄位）

MAGNESIUM CHLORIDE HEXAHYDRATE (EQ TO MAGNESIUM CHLORIDE 6H2O);;MAGNESIUM CHLORIDE HEXAHYDRATE (EQ TO MAGNESIUM CHLORIDE 6H2O);;SODIUM S-LACTATE SOLUTION 50%;;SODIUM CHLORIDE;;SODIUM CHLORIDE;;SODIUM LACTATE;;CALCIUM CHLORIDE DIHYDRATE;;CALCIUM CHLORIDE DIHYDRATE;;GLUCOSE MONOHYDRATE;;GLUCOSE MONOHYDRATE