MR编号 | CZ/H/0231/001 |
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药品名称 | LORISTA H 100 mg/12.5 mg |
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活性成分 | - Hydrochlorothiazide 12.5 mg
- Losartan 100.0 mg
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剂型 | Film-coated tablet |
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上市许可持有人 | Krka d.d., Novo mesto, Novo mesto,Slovenia |
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参考成员国 - 产品名称 | Czechia (CZ) |
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互认成员国 - 产品名称 | - Germany (DE)
Losartan-Kalium HCTad 100mg/12,5mg Filmtabletten - Denmark (DK)
- United Kingdom (Northern Ireland) (XI)
- Austria (AT)
Losartan/HCT Krka 100 mg/12,5 mg Filmtabletten - Spain (ES)
- Portugal (PT)
- Italy (IT)
- Sweden (SE)
- Norway (NO)
- Finland (FI)
- Poland (PL)
- Latvia (LV)
- Lithuania (LT)
Lorista H 100 mg/12,5 mg plėvele dengtos tabletės - Estonia (EE)
LORISTA H 100MG/12,5MG - Hungary (HU)
LAVESTRA H 100 mg/12,5 mg filmtabletta - Bulgaria (BG)
Lorista HL - Iceland (IS)
- Cyprus (CY)
LOSARTAN /HCT KRKA 100mg/12,5mg FC TABS - Romania (RO)
Lorista HL 100 mg / 12,5 mg comprimate filmate - Slovakia (SK)
Lorista H 100 mg/ 12,5 mg
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许可日期 | 2010/07/16 |
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最近更新日期 | 2025/01/20 |
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药物ATC编码 | - C09DA01 losartan and diuretics
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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
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附件文件下载 | |
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市场状态 | Positive |
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