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 |
2023/07/18 |
SUPPL-38(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2023/04/13 |
SUPPL-37(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/03/04 |
SUPPL-35(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2020/11/27 |
SUPPL-34(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2020/09/11 |
SUPPL-31(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/06/07 |
SUPPL-30(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/06/07 |
SUPPL-29(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/10/17 |
SUPPL-27(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/10/24 |
SUPPL-26(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/10/24 |
SUPPL-25(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/07/08 |
SUPPL-23(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
2016/07/08 |
SUPPL-22(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
2016/07/08 |
SUPPL-21(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
2016/02/02 |
SUPPL-20(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2015/12/16 |
SUPPL-18(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/12/19 |
SUPPL-19(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2013/08/20 |
SUPPL-17(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2012/12/20 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2012/09/28 |
SUPPL-14(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2012/05/03 |
SUPPL-15(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2011/10/28 |
SUPPL-11(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2011/06/17 |
SUPPL-8(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
2011/05/20 |
SUPPL-12(补充) |
Approval |
Labeling |
901 REQUIRED
|
|
|
2011/04/07 |
SUPPL-7(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2010/09/03 |
SUPPL-5(补充) |
Approval |
Labeling |
901 REQUIRED
|
|
|
2010/06/22 |
SUPPL-2(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2010/03/19 |
SUPPL-4(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2010/03/19 |
SUPPL-3(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2009/01/30 |
ORIG-1(原始申请) |
Approval |
Type 2 - New Active Ingredient |
STANDARD
|
|
|
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:DEXLANSOPRAZOLE 剂型/给药途径:CAPSULE, DELAYED RELEASE;ORAL 规格:30MG 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 |
022287 |
001 |
NDA |
DEXILANT |
DEXLANSOPRAZOLE |
CAPSULE, DELAYED RELEASE;ORAL |
30MG |
Prescription |
Yes |
No |
AB |
2009/01/30
|
TAKEDA PHARMS USA |
202294 |
002 |
ANDA |
DEXLANSOPRAZOLE |
DEXLANSOPRAZOLE |
CAPSULE, DELAYED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2022/06/16
|
ENDO OPERATIONS |
202666 |
001 |
ANDA |
DEXLANSOPRAZOLE |
DEXLANSOPRAZOLE |
CAPSULE, DELAYED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2022/09/16
|
TWI PHARMS |
205205 |
001 |
ANDA |
DEXLANSOPRAZOLE |
DEXLANSOPRAZOLE |
CAPSULE, DELAYED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2024/01/19
|
MYLAN |
活性成分:DEXLANSOPRAZOLE 剂型/给药途径:CAPSULE, DELAYED RELEASE;ORAL 规格:60MG 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 |
022287 |
002 |
NDA |
DEXILANT |
DEXLANSOPRAZOLE |
CAPSULE, DELAYED RELEASE;ORAL |
60MG |
Prescription |
Yes |
Yes |
AB |
2009/01/30
|
TAKEDA PHARMS USA |
202294 |
001 |
ANDA |
DEXLANSOPRAZOLE |
DEXLANSOPRAZOLE |
CAPSULE, DELAYED RELEASE;ORAL |
60MG |
Prescription |
No |
No |
AB |
2017/04/19
|
ENDO OPERATIONS |
202666 |
002 |
ANDA |
DEXLANSOPRAZOLE |
DEXLANSOPRAZOLE |
CAPSULE, DELAYED RELEASE;ORAL |
60MG |
Prescription |
No |
No |
AB |
2022/09/16
|
TWI PHARMS |
205205 |
002 |
ANDA |
DEXLANSOPRAZOLE |
DEXLANSOPRAZOLE |
CAPSULE, DELAYED RELEASE;ORAL |
60MG |
Prescription |
No |
No |
AB |
2024/01/19
|
MYLAN |