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 |
| 2005/07/22 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
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 |
| 2021/11/03 |
SUPPL-22(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2018/12/21 |
SUPPL-21(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2016/07/13 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2013/06/14 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2012/03/01 |
SUPPL-14(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2012/03/01 |
SUPPL-6(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2012/02/21 |
SUPPL-12(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2011/08/04 |
SUPPL-15(补充) |
Approval |
REMS-Modified |
N/A
|
|
|
| 2010/11/09 |
SUPPL-11(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2008/10/20 |
SUPPL-10(补充) |
Approval |
Efficacy-Labeling Change With Clinical Data |
UNKNOWN
|
|
|
| 2008/10/20 |
SUPPL-9(补充) |
Approval |
Efficacy-Labeling Change With Clinical Data |
UNKNOWN
|
|
|
| 2008/10/20 |
SUPPL-8(补充) |
Approval |
REMS-Proposal,Efficacy-Labeling Change With Clinical Data |
UNKNOWN
|
|
|
| 2005/08/18 |
SUPPL-1(补充) |
Approval |
Labeling |
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:RAMELTEON; 剂型/给药途径:TABLET;ORAL; 规格:8MG; 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 |
| 021782 |
001 |
NDA |
ROZEREM |
RAMELTEON |
TABLET;ORAL |
8MG |
Prescription |
Yes |
Yes |
AB |
2005/07/22
|
TAKEDA PHARMS USA |
| 091693 |
001 |
ANDA |
RAMELTEON |
RAMELTEON |
TABLET;ORAL |
8MG |
Prescription |
No |
No |
AB |
2013/07/26
|
DR REDDYS LABS SA |
| 091610 |
001 |
ANDA |
RAMELTEON |
RAMELTEON |
TABLET;ORAL |
8MG |
Prescription |
No |
No |
AB |
2015/08/19
|
ACTAVIS LABS FL INC |
| 211567 |
001 |
ANDA |
RAMELTEON |
RAMELTEON |
TABLET;ORAL |
8MG |
Prescription |
No |
No |
AB |
2019/07/22
|
ZYDUS PHARMS |
| 213186 |
001 |
ANDA |
RAMELTEON |
RAMELTEON |
TABLET;ORAL |
8MG |
Discontinued |
No |
No |
AB |
2020/08/21
|
GRANULES |
| 213815 |
001 |
ANDA |
RAMELTEON |
RAMELTEON |
TABLET;ORAL |
8MG |
Prescription |
No |
No |
AB |
2020/10/26
|
APPCO |
| 215435 |
001 |
ANDA |
RAMELTEON |
RAMELTEON |
TABLET;ORAL |
8MG |
Prescription |
No |
No |
AB |
2022/08/24
|
ANDAS 5 HOLDING |
| 215243 |
001 |
ANDA |
RAMELTEON |
RAMELTEON |
TABLET;ORAL |
8MG |
Prescription |
No |
No |
AB |
2023/02/09
|
MICRO LABS |