| MR编号 | NL/H/5049/001 |
|---|
| 药品名称 | Abirateron Sandoz 1000 mg, filmomhulde tabletten |
|---|
| 活性成分 | - abiraterone acetate 1000.0 mg
|
|---|
| 剂型 | Film-coated tablet |
|---|
| 上市许可持有人 | Sandoz B.V.
Veluwezoom 22
1327 AH Almere
Netherlands |
|---|
| 参考成员国 - 产品名称 | Netherlands (NL) Abirateron Sandoz 1000 mg, filmomhulde tabletten |
|---|
| 互认成员国 - 产品名称 | - United Kingdom (Northern Ireland) (XI)
- Sweden (SE)
- Norway (NO)
Abirateron Sandoz - Finland (FI)
- Poland (PL)
Abiraterone Sandoz - Germany (DE)
Abirateron Hexal 1000 mg Filmtabletten - Latvia (LV)
Abiraterone Sandoz 1000 mg apvalkotās tabletes - Denmark (DK)
- 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)
|
|---|
| 许可日期 | 2021/05/12 |
|---|
| 最近更新日期 | 2024/04/29 |
|---|
| 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
|
|---|
| 附件文件下载 | |
|---|
| 市场状态 | Positive |
|---|
|
|---|