欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
BE/H/0277/001
药品名称
Duogestan 1mg/200mg
活性成分
estradiol hemihydrate 1.0 mg
progesterone 200.0 mg
剂型
capsule soft und tablet
上市许可持有人
Besins Healthcare SA Avenue Louise 287 1050 Brussels Belgium
参考成员国 - 产品名称
Belgium (BE)
互认成员国 - 产品名称
Bulgaria (BG)
DUOGESTAN 1 mg/ 200 mg
Czechia (CZ)
Duogestan 1mg/200mg
Croatia (HR)
Duogestan 1 mg/200 mg tableta i meka kapsula
Estonia (EE)
Germany (DE)
Duogestan 1 mg/200 mg
Hungary (HU)
Ireland (IE)
Lithuania (LT)
-
Latvia (LV)
Netherlands (NL)
Poland (PL)
Duogestan
Romania (RO)
Duogestan 1 mg/200 mg
Slovenia (SI)
Slovakia (SK)
United Kingdom (GB)
许可日期
2020/12/22
最近更新日期
2021/11/15
药物ATC编码
G03FA04 progesterone and estrogen
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Bibliographic Art 10 a Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
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