欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/0296/001
药品名称
Ticlopidin-Teva
活性成分
ticlopidine hydrochloride 250.0 mg
剂型
Film-coated tablet
上市许可持有人
TEVA GmbH Graf-Arco-Str. 3 D-89079 Ulm
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
许可日期
2001/08/13
最近更新日期
2013/05/29
药物ATC编码
B01AC05 ticlopidine
申请类型
TypeLevel1:
Abridged
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
|
DE_Ticlopidin Teva_GI_44855 00 00_02 05 12 vs 03_2010 _2_ clean
Date of last change:2024/09/06
Final SPC
|
TiclopidineTeva_ BE SPCNL_clean
Date of last change:2024/09/06
Final SPC
|
TiclopidineTeva_BE PILDE_clean
Date of last change:2024/09/06
Final SPC
|
TiclopidineTeva_BE PILFR_clean
Date of last change:2024/09/06
Final SPC
|
TiclopidineTeva_BE PILNL_clean
Date of last change:2024/09/06
Final SPC
|
TiclopidineTeva_BE SPCFR_clean
Date of last change:2024/09/06
Final SPC
|
TiclopidineTeva_labelling_BE_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase