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
提交状态日期 | 提交号 | 审批结论 | 申请内容分类 | 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 |
2024/09/16 |
SUPPL-34(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2021/06/07 |
SUPPL-29(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2007/12/26 |
SUPPL-23(补充) |
Approval |
Labeling |
|
|
|
2002/04/10 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2001/12/14 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2001/10/26 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
2000/05/16 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2000/01/24 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/12/21 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/09/24 |
SUPPL-17(补充) |
Approval |
Labeling |
|
|
|
1999/07/07 |
SUPPL-14(补充) |
Approval |
Labeling |
|
|
|
1999/05/20 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/03/26 |
SUPPL-12(补充) |
Approval |
Labeling |
|
|
|
1999/03/26 |
SUPPL-11(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/03/11 |
SUPPL-7(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/02/05 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/12/01 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/09/25 |
SUPPL-6(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/09/25 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1996/12/27 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1996/08/09 |
ORIG-1(原始申请) |
Approval |
|
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号 | 专利号 | 专利过期日 | 是否物质专利 | 是否产品专利 | 专利用途代码 | 撤销请求 | 提交日期 | 专利下载 | 备注 |
无 |
与本品治疗等效的药品
活性成分:MEDROXYPROGESTERONE ACETATE 剂型/给药途径:TABLET;ORAL 规格:2.5MG 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 |
011839 |
001 |
NDA |
PROVERA |
MEDROXYPROGESTERONE ACETATE |
TABLET;ORAL |
2.5MG |
Prescription |
Yes |
No |
AB |
Approved Prior to Jan 1, 1982
|
PFIZER |
040159 |
001 |
ANDA |
MEDROXYPROGESTERONE ACETATE |
MEDROXYPROGESTERONE ACETATE |
TABLET;ORAL |
2.5MG |
Prescription |
No |
No |
AB |
1996/08/09
|
BARR |
活性成分:MEDROXYPROGESTERONE ACETATE 剂型/给药途径:TABLET;ORAL 规格:5MG 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 |
011839 |
003 |
NDA |
PROVERA |
MEDROXYPROGESTERONE ACETATE |
TABLET;ORAL |
5MG |
Prescription |
Yes |
No |
AB |
Approved Prior to Jan 1, 1982
|
PFIZER |
040159 |
002 |
ANDA |
MEDROXYPROGESTERONE ACETATE |
MEDROXYPROGESTERONE ACETATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AB |
1996/08/09
|
BARR |
活性成分:MEDROXYPROGESTERONE ACETATE 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 |
011839 |
004 |
NDA |
PROVERA |
MEDROXYPROGESTERONE ACETATE |
TABLET;ORAL |
10MG |
Prescription |
Yes |
Yes |
AB |
Approved Prior to Jan 1, 1982
|
PFIZER |
040159 |
003 |
ANDA |
MEDROXYPROGESTERONE ACETATE |
MEDROXYPROGESTERONE ACETATE |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AB |
1996/08/09
|
BARR |