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 |
2016/09/26 |
SUPPL-40(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2016/01/04 |
SUPPL-46(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/01/04 |
SUPPL-45(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/07/05 |
SUPPL-38(补充) |
Approval |
Labeling |
|
|
|
2001/04/11 |
SUPPL-37(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2001/03/07 |
SUPPL-35(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2001/03/07 |
SUPPL-34(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2000/04/17 |
SUPPL-36(补充) |
Approval |
Labeling |
|
|
|
1998/10/01 |
SUPPL-33(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1997/03/03 |
SUPPL-32(补充) |
Approval |
Labeling |
|
|
|
1994/04/12 |
SUPPL-31(补充) |
Approval |
Labeling |
|
|
|
1994/04/12 |
SUPPL-30(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1993/06/16 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1993/06/16 |
SUPPL-23(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1993/06/16 |
SUPPL-22(补充) |
Approval |
Labeling |
|
|
|
1993/06/16 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1992/12/04 |
SUPPL-29(补充) |
Approval |
Labeling |
|
|
|
1991/05/13 |
SUPPL-28(补充) |
Approval |
Labeling |
|
|
|
1991/02/13 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1988/10/14 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
1987/10/26 |
ORIG-1(原始申请) |
Approval |
|
|
|
|
1987/05/15 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/05/15 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1984/08/10 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1984/05/11 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1983/02/28 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1982/03/10 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
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:ISOSORBIDE DINITRATE 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 |
086923 |
001 |
ANDA |
ISOSORBIDE DINITRATE |
ISOSORBIDE DINITRATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AB |
1987/03/12
|
ENDO OPERATIONS |
086067 |
001 |
ANDA |
ISOSORBIDE DINITRATE |
ISOSORBIDE DINITRATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AB |
1987/10/29
|
HIKMA INTL PHARMS |
086221 |
001 |
ANDA |
ISOSORBIDE DINITRATE |
ISOSORBIDE DINITRATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AB |
1988/01/07
|
SANDOZ |
012093 |
007 |
NDA |
ISORDIL |
ISOSORBIDE DINITRATE |
TABLET;ORAL |
5MG |
Prescription |
Yes |
No |
AB |
1988/07/29
|
BAUSCH |
213057 |
001 |
ANDA |
ISOSORBIDE DINITRATE |
ISOSORBIDE DINITRATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AB |
2019/11/20
|
ZYDUS LIFESCIENCES |
215723 |
001 |
ANDA |
ISOSORBIDE DINITRATE |
ISOSORBIDE DINITRATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AB |
2022/07/08
|
RUBICON |