欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0775/002
药品名称
Meropenem Teva
活性成分
meropenem trihydrate 1000.0 mg
剂型
Powder for solution for infusion/injection
上市许可持有人
Teva Pharma - Prod. Farmacêuticos, Lda
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
France (FR)
Greece (GR)
Hungary (HU)
MEROPENEM Teva 500 mg és 1000 mg por oldatos injekcióhoz vagy infúzióhoz
许可日期
2013/03/28
最近更新日期
2016/09/27
药物ATC编码
J01DH02 meropenem
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Labelling
|
1_3_1 label_inner_vial__meropenem 500 and 1000 mg_clean
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label_outer_meropenem 500 and 1000mg_clean
Date of last change:2024/09/06
Final PL
|
1_3_1 meropenem_500 and 1000 mg_pil_clean
Date of last change:2024/09/06
Final SPC
|
1_3_1 meropenem_500 and 1000 mg_spc_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase