欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/0309/001
药品名称
Pentastarch 6%
活性成分
poly(O-2-hydroxyethyl)starch sodium chloride 69.0 g
剂型
Solution for infusion
上市许可持有人
Baxter Deutschland GmbH Edisonstraße 4 85716 Unterschleißheim
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Belgium (BE)
Portugal (PT)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Pentastarch 6 % "Baxter" - Infusionslösung
France (FR)
Italy (IT)
许可日期
2001/11/29
最近更新日期
2012/08/10
药物ATC编码
B05AA07 hydroxyethylstarch
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Generic Article 4.8(a)(iii), first paragraph
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final SPC
|
spcen-pentastarch-10-renewal-1006
Date of last change:2010/07/23
Final SPC
|
spcen-pentastarch-6-renewal-1006
Date of last change:2010/07/23
Final Labelling
|
labip-001-pentastarch-10-renewal-1006
Date of last change:2010/07/23
Final Labelling
|
labip-001-pentastarch-6-renewal-090227-1
Date of last change:2010/07/23
Final Labelling
|
labop-001-pentastarch-10-renewal-090227-1
Date of last change:2010/07/23
Final Labelling
|
labop-001-pentastarch-6-renewal-090227
Date of last change:2010/07/23
Final PL
|
palen-pentastarch-10-renewal-1006
Date of last change:2010/07/23
Final PL
|
palen-pentastarch-6-renewal-1006
Date of last change:2010/07/23
市场状态
Positive
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