雲析藥典

TFDA 藥品許可證

百源雙利-1號

PN-TWIN NO.1

已註銷

基本資料

許可證字號
衛署藥輸字第023171號
許可證種類
製 劑
劑型
注射劑
藥品類別
限由醫師使用
管制藥品級別
法規處分狀態
已註銷
效期狀態
已逾效期
狀態基準日
2026-08-16
發證日期
2001-04-30
有效期限
2006-04-30
異動日期
2004-07-08

詳細處方成分

EACH 800ML CONTAINS (COMPARTMENT-I):GLUCOSE4020000700120.0(結構化:120.000000 GM)
EACH 800ML CONTAINS (COMPARTMENT-I):SODIUM CHLORIDE40120021002.920(結構化:2.920000 GM)
EACH 800ML CONTAINS (COMPARTMENT-I):POTASSIUM ACETATE40080001002.160(結構化:2.160000 GM)
EACH 800ML CONTAINS (COMPARTMENT-I):MAGNESIUM SULFATE56120015000.740(結構化:0.740000 GM)
EACH 800ML CONTAINS (COMPARTMENT-I):CALCIUM GLUCONATE68240001001.792(結構化:1.792000 GM)
EACH 800ML CONTAINS (COMPARTMENT-I):ZINC SULFATE92000106005.752(結構化:5.752000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-ISOLEUCINE40201010021.120(結構化:1.120000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-ARGININE40201003021.580(結構化:1.580000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-ASPARTIC ACID40201004020.760(結構化:0.760000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-CYSTEINE40201005020.200(結構化:0.200000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):GLUTAMIC ACID L-40201007021.300(結構化:1.300000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-HISTIDINE40201009021.200(結構化:1.200000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-PROLINE40201018020.660(結構化:0.660000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-SERINE40201019020.440(結構化:0.440000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-TYROSINE40201022020.070(結構化:0.070000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):GLYCINE (EQ TO AMINOACETIC ACID)(EQ TO GLYCOCOLL)40201024002.140(結構化:2.140000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-LEUCINE40201012022.500(結構化:2.500000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-LYSINE ACETATE40201013222.480(結構化:2.480000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-METHIONINE40201015020.700(結構化:0.700000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-PHENYLALANINE40201017021.870(結構化:1.870000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-THREONINE40201020021.300(結構化:1.300000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-TRYPTOPHAN40201021020.260(結構化:0.260000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-VALINE40201023020.900(結構化:0.900000 GM)
EACH 200ML CONTAINS (COMPARTMENT-II):L-ALANINE40201002021.240(結構化:1.240000 GM)

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)

POTASSIUM PHOSPHATE MONOBASIC(EQ TO POTASSIUM BIPHOSPHATE)(EQ TO POTASSIUM DIHYDROGEN PHOSPHATE);;L-PHENYLALANINE;;L-TRYPTOPHAN;;L-THREONINE;;L-VALINE;;L-METHIONINE;;SODIUM CHLORIDE;;L-ARGININE;;GLUTAMIC ACID L-;;L-ALANINE;;L-ISOLEUCINE;;ZINC SULFATE;;L-PROLINE;;CALCIUM GLUCONATE;;L-CYSTEINE;;L-SERINE;;POTASSIUM ACETATE;;MAGNESIUM SULFATE;;L-HISTIDINE;;L-LEUCINE;;L-ASPARTIC ACID;;L-LYSINE ACETATE;;L-TYROSINE;;GLUCOSE;;GLYCINE (EQ TO AMINOACETIC ACID)(EQ TO GLYCOCOLL)

適應症

對於不能經口及?或經腸道攝取營養或營養攝取不足的病人,以中心靜脈營養輸注方式補充水份、電解質、氨基酸及熱量。

官方用法用量

官方資料未提供

包裝

塑膠軟袋裝;;袋裝

註銷/廢止資訊

註銷狀態原文
已註銷
日期
2004-07-07
原因
自請註銷

申請商與製造資料

申請商
中國化學製藥股份有限公司
申請商地址
台北巿襄陽路23號
製造商
AJINOMOTO PHARMA CO., LTD. SAITAMA FACTORY
製造廠址
6-8 HACHIMAN KAWAJIMA-MACHI HIKI-GUM SAITAMA 350-0151 JAPAN
製造國別
JP
製程

來源與版本

資料集
全部藥品許可證資料集
擷取時間
2026/8/15 上午4:23:47
SHA-256
caf5b2bf2ea2c2d0f77c290d5adff2b2dd12ddb104ea50c8cf6909c0982f09c0
開啟官方資料集 ↗

來源與版本

資料集
未註銷藥品許可證資料集(狀態判定)
擷取時間
2026/8/15 下午7:17:55
SHA-256
f73c236f0fc914c40cbfdfa5eb0914ff058d5acb2a6945b01a49c644176f09e5
開啟官方資料集 ↗

狀態規則:tfda-license-lifecycle-2026-08-16.1。只有列於未註銷名單且仍在有效日期內,才顯示為有效。

本頁呈現官方來源原始欄位,不等於經臨床編審的完整藥典,也不得取代醫師或藥師的專業判斷。