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 |
| 2010/02/10 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
STANDARD
|
|
|
>>>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 |
| 2022/12/15 |
SUPPL-25(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2020/10/21 |
SUPPL-24(补充) |
Approval |
Labeling-Package Insert,Labeling-Patient Package Insert |
STANDARD
|
|
|
| 2019/12/19 |
SUPPL-23(补充) |
Approval |
Labeling-Patient Package Insert,Labeling-Package Insert |
STANDARD
|
|
|
| 2019/08/21 |
SUPPL-22(补充) |
Approval |
Labeling-Patient Package Insert,Labeling-Package Insert |
STANDARD
|
|
|
| 2018/11/15 |
SUPPL-21(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2017/09/29 |
SUPPL-20(补充) |
Approval |
Labeling-Package Insert,Labeling-Patient Package Insert |
STANDARD
|
|
|
| 2017/06/29 |
SUPPL-18(补充) |
Approval |
Labeling-Package Insert,Labeling-Medication Guide |
STANDARD
|
|
|
| 2017/06/07 |
SUPPL-19(补充) |
Approval |
Labeling-Package Insert,Labeling-Patient Package Insert |
STANDARD
|
|
|
| 2016/12/22 |
SUPPL-16(补充) |
Approval |
Labeling-Package Insert,Labeling-Patient Package Insert |
STANDARD
|
|
|
| 2016/11/22 |
SUPPL-15(补充) |
Approval |
Labeling-Package Insert,Labeling-Patient Package Insert |
STANDARD
|
|
|
| 2016/09/15 |
SUPPL-17(补充) |
Approval |
Labeling-Package Insert |
901 REQUIRED
|
|
|
| 2015/11/10 |
SUPPL-14(补充) |
Approval |
Labeling-Package Insert,Labeling-Patient Package Insert |
STANDARD
|
|
|
| 2015/03/27 |
SUPPL-13(补充) |
Approval |
Labeling-Package Insert |
901 REQUIRED
|
|
|
| 2015/03/16 |
SUPPL-12(补充) |
Approval |
Labeling-Package Insert,Labeling-Medication Guide |
STANDARD
|
|
|
| 2013/11/07 |
SUPPL-10(补充) |
Approval |
Labeling-Patient Package Insert,Labeling-Package Insert |
STANDARD
|
|
|
| 2012/11/20 |
SUPPL-8(补充) |
Approval |
Labeling-Package Insert,Labeling-Patient Package Insert |
STANDARD
|
|
|
| 2012/02/17 |
SUPPL-7(补充) |
Approval |
Labeling-Patient Package Insert |
901 REQUIRED
|
|
|
| 2011/12/06 |
SUPPL-6(补充) |
Approval |
Labeling-Patient Package Insert,Labeling-Package Insert |
STANDARD
|
|
|
| 2010/04/27 |
SUPPL-1(补充) |
Approval |
Labeling-Package Insert |
901 REQUIRED
|
|
|
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:RITONAVIR; 剂型/给药途径:TABLET;ORAL; 规格:100MG; 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 |
| 022417 |
001 |
NDA |
NORVIR |
RITONAVIR |
TABLET;ORAL |
100MG |
Prescription |
Yes |
Yes |
AB |
2010/02/10
|
ABBVIE |
| 202573 |
001 |
ANDA |
RITONAVIR |
RITONAVIR |
TABLET;ORAL |
100MG |
Prescription |
No |
No |
AB |
2015/01/15
|
CIPLA |
| 204587 |
001 |
ANDA |
RITONAVIR |
RITONAVIR |
TABLET;ORAL |
100MG |
Prescription |
No |
No |
AB |
2018/09/17
|
HETERO LABS LTD III |
| 206614 |
001 |
ANDA |
RITONAVIR |
RITONAVIR |
TABLET;ORAL |
100MG |
Prescription |
No |
No |
AB |
2018/09/17
|
AUROBINDO PHARMA LTD |
| 208890 |
001 |
ANDA |
RITONAVIR |
RITONAVIR |
TABLET;ORAL |
100MG |
Prescription |
No |
No |
AB |
2018/09/17
|
AMNEAL |
| 203759 |
001 |
ANDA |
RITONAVIR |
RITONAVIR |
TABLET;ORAL |
100MG |
Prescription |
No |
No |
AB |
2022/05/10
|
CIPLA |