| MR编号 | NL/H/5049/001 |
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| 药品名称 | Abirateron Sandoz 1000 mg, filmomhulde tabletten |
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| 活性成分 | - Abiraterone acetate 1000.0 mg
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| 剂型 | Film-coated tablet |
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| 上市许可持有人 | Sandoz B.V.
Veluwezoom 22
1327 AH Almere
Netherlands |
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| 参考成员国 - 产品名称 | Netherlands (NL) Abirateron Sandoz 1000 mg, filmomhulde tabletten |
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| 互认成员国 - 产品名称 | - United Kingdom (Northern Ireland) (XI)
- Poland (PL)
Abiraterone Sandoz - Germany (DE)
Abirateron Hexal 1000 mg Filmtabletten - Latvia (LV)
Abiraterone Sandoz 1000 mg apvalkotās tabletes - Lithuania (LT)
Abiraterone Ebewe 1000 mg plėvele dengtos tabletės - Austria (AT)
Abirateron Sandoz 1000 mg – Filmtabletten - Estonia (EE)
ABIRATERONE SANDOZ - France (FR)
- Hungary (HU)
- Spain (ES)
- Czechia (CZ)
Abiraterone Sandoz - Portugal (PT)
- Slovakia (SK)
Abiraterón Sandoz 1000 mg filmom obalené tablety - Italy (IT)
- Croatia (HR)
Abirateron Sandoz 1000 mg filmom obložene tablete - Greece (GR)
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| 许可日期 | 2021/05/12 |
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| 最近更新日期 | 2025/09/22 |
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| 药物ATC编码 | | 申请类型 | - TypeLevel1：Abridged
- TypeLevel2：Initial Application
- TypeLevel3：Other Generic application Art 10.3 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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