批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
>>>原始批准或临时批准<<<
| 审批日期 | 提交号 | 审批结论 | 提交分类 | 审评优先级;罕用药状态 | 通知信、审评文件、说明书、包装标签 | 备注 |
| 2013/10/18 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
STANDARD
;Orphan
|
|
|
>>>补充申请<<<
| 审批日期 | 提交号 | 审批结论 | 补充类别或审批类型 | 审评优先级;罕用药状态 | 通知信、审评文件、说明书、包装标签 | 备注 |
| 2025/04/02 |
SUPPL-31(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
;Orphan
|
|
|
| 2025/02/28 |
SUPPL-29(补充) |
Approval |
Efficacy-Labeling Change With Clinical Data |
PRIORITY
;Orphan
|
|
|
| 2024/12/12 |
SUPPL-30(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
|
|
|
| 2024/04/11 |
SUPPL-27(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
|
|
|
| 2023/05/26 |
SUPPL-24(补充) |
Approval |
Labeling-Package Insert |
STANDARD
;Orphan
|
|
|
| 2023/02/01 |
SUPPL-23(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
|
|
|
| 2021/10/25 |
SUPPL-22(补充) |
Approval |
Labeling-Package Insert |
STANDARD
;Orphan
|
|
|
| 2021/05/26 |
SUPPL-21(补充) |
Approval |
Labeling-Package Insert |
STANDARD
;Orphan
|
|
|
| 2020/04/08 |
SUPPL-20(补充) |
Approval |
REMS - MODIFIED - D-N-A,REMS - MODIFIED - BIFURCATED |
N/A
;Orphan
|
|
|
| 2019/06/10 |
SUPPL-19(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
;Orphan
|
|
|
| 2019/04/23 |
SUPPL-17(补充) |
Approval |
Labeling-Package Insert |
STANDARD
;Orphan
|
|
|
| 2019/02/01 |
SUPPL-18(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
;Orphan
|
|
|
| 2018/10/16 |
SUPPL-10(补充) |
Approval |
Labeling-Medication Guide |
STANDARD
|
|
|
| 2017/08/25 |
SUPPL-13(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
|
|
|
| 2017/03/21 |
SUPPL-11(补充) |
Approval |
Labeling-Package Insert,Labeling-Medication Guide |
STANDARD
;Orphan
|
|
|
| 2016/10/21 |
SUPPL-9(补充) |
Approval |
Labeling-Package Insert |
STANDARD
;Orphan
|
|
|
| 2016/06/15 |
SUPPL-8(补充) |
Approval |
Labeling-Package Insert |
STANDARD
;Orphan
|
|
|
| 2016/03/22 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2016/02/22 |
SUPPL-7(补充) |
Approval |
REMS-Modified |
N/A
;Orphan
|
|
|
| 2016/02/17 |
SUPPL-6(补充) |
Approval |
Labeling-Package Insert |
STANDARD
;Orphan
|
|
|
| 2015/11/17 |
SUPPL-2(补充) |
Approval |
REMS-Modified |
N/A
;Orphan
|
|
|
| 2015/04/30 |
SUPPL-3(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2014/05/20 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
;Orphan
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
与本品治疗等效的药品
>>>活性成分:MACITENTAN; 剂型/给药途径:TABLET;ORAL; 规格:10MG; 治疗等效代码:AB<<<
| 申请号 | 产品号 | 申请类型 | 商品名 | 活性成分 | 剂型/给药途径 | 规格 | 市场状态 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
| 204410 |
001 |
NDA |
OPSUMIT |
MACITENTAN |
TABLET;ORAL |
10MG |
Prescription |
Yes |
Yes |
AB |
2013/10/18
|
ACTELION |
| 211198 |
001 |
ANDA |
MACITENTAN |
MACITENTAN |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AB |
2023/04/18
|
AUROBINDO PHARMA LTD |
| 211195 |
001 |
ANDA |
MACITENTAN |
MACITENTAN |
TABLET;ORAL |
10MG |
Discontinued |
No |
No |
AB |
2024/01/09
|
APOTEX |
| 211107 |
001 |
ANDA |
MACITENTAN |
MACITENTAN |
TABLET;ORAL |
10MG |
Discontinued |
No |
No |
AB |
2024/08/05
|
TORRENT |
| 211128 |
001 |
ANDA |
MACITENTAN |
MACITENTAN |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AB |
2025/08/18
|
ALEMBIC |
| 211136 |
001 |
ANDA |
MACITENTAN |
MACITENTAN |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AB |
2025/08/20
|
MSN |
| 211123 |
001 |
ANDA |
MACITENTAN |
MACITENTAN |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AB |
2025/08/26
|
SUN PHARM |
| 211120 |
001 |
ANDA |
MACITENTAN |
MACITENTAN |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AB |
2025/11/05
|
LAURUS |