欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IT/H/0736/001
药品名称
CLINIMIX
活性成分
alanine 0.0 %
arginine 0.0 %
calcium chloride anhydrous monohydrate 0.0 %
calcium chloride anhydrous 0.0 %
glucose monohydrate 0.0 %
glycine 0.0 %
histidine 0.0 %
isoleucine 0.0 %
leucine 0.0 %
lysine hydrochloride 0.0 %
magnesium chloride hexahydrate 0.0 %
methionine 0.0 %
phenylalanine 0.0 %
proline 0.0 %
serine 0.0 %
sodium acetate 0.0 %
sodium chloride 0.0 %
threonine 0.0 %
tryptophan 0.0 %
tyrosine 0.0 %
剂型
Solution for infusion
上市许可持有人
Baxter S.p.A. Piazzale Dell'Industria 20 00144 - Rome Italy
参考成员国 - 产品名称
Italy (IT)
互认成员国 - 产品名称
Denmark (DK)
United Kingdom (Northern Ireland) (XI)
Belgium (BE)
Netherlands (NL)
France (FR)
Poland (PL)
Finland (FI)
Cyprus (CY)
Czechia (CZ)
Luxembourg (LU)
Austria (AT)
Clinimix 3 % G-E - Infusionsbeutel
Spain (ES)
Sweden (SE)
许可日期
2008/04/05
最近更新日期
2024/06/21
药物ATC编码
B05BA10 combinations
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final Labelling
|
common_outer_clean
Date of last change:2024/09/06
Final PL
|
common_pl_WS 58 Clinimix_
Date of last change:2024/09/06
Final SPC
|
common_spc WS 58 Clinimix
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase