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 |
2016/11/30 |
SUPPL-8(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2012/03/15 |
SUPPL-7(补充) |
Approval |
Labeling |
|
|
|
2012/03/15 |
SUPPL-5(补充) |
Approval |
Labeling |
|
|
|
2011/09/29 |
SUPPL-6(补充) |
Approval |
Labeling |
|
|
|
2011/01/12 |
SUPPL-4(补充) |
Approval |
Labeling |
|
|
|
2010/02/23 |
SUPPL-3(补充) |
Approval |
Labeling |
|
|
|
2009/09/21 |
SUPPL-2(补充) |
Approval |
Labeling |
|
|
|
2009/09/21 |
SUPPL-1(补充) |
Approval |
Labeling |
|
|
|
2009/01/22 |
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:LAMOTRIGINE 剂型/给药途径:TABLET, FOR SUSPENSION;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 |
020764 |
001 |
NDA |
LAMICTAL CD |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
5MG |
Prescription |
Yes |
No |
AB |
1998/08/24
|
GLAXOSMITHKLINE LLC |
076701 |
001 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
5MG |
Prescription |
No |
No |
AB |
2009/01/22
|
DR REDDYS LABS LTD |
076928 |
002 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
5MG |
Prescription |
No |
No |
AB |
2009/01/22
|
WATSON LABS |
078009 |
002 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
5MG |
Prescription |
No |
No |
AB |
2009/01/22
|
ZYDUS PHARMS USA INC |
079204 |
001 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
5MG |
Prescription |
No |
No |
AB |
2009/02/04
|
TARO |
079099 |
001 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
5MG |
Prescription |
No |
No |
AB |
2009/02/19
|
GLENMARK PHARMS LTD |
090401 |
002 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
5MG |
Prescription |
No |
No |
AB |
2009/11/04
|
AUROBINDO PHARMA |
201168 |
001 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
5MG |
Prescription |
No |
No |
AB |
2014/06/12
|
ALEMBIC |
活性成分:LAMOTRIGINE 剂型/给药途径:TABLET, FOR SUSPENSION;ORAL 规格:25MG 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 |
020764 |
002 |
NDA |
LAMICTAL CD |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
25MG |
Prescription |
Yes |
Yes |
AB |
1998/08/24
|
GLAXOSMITHKLINE LLC |
076701 |
002 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
25MG |
Prescription |
No |
No |
AB |
2009/01/22
|
DR REDDYS LABS LTD |
076928 |
003 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
25MG |
Prescription |
No |
No |
AB |
2009/01/22
|
WATSON LABS |
078009 |
003 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
25MG |
Prescription |
No |
No |
AB |
2009/01/22
|
ZYDUS PHARMS USA INC |
079204 |
002 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
25MG |
Prescription |
No |
No |
AB |
2009/02/04
|
TARO |
079099 |
002 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
25MG |
Prescription |
No |
No |
AB |
2009/02/19
|
GLENMARK PHARMS LTD |
090401 |
003 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
25MG |
Prescription |
No |
No |
AB |
2009/11/04
|
AUROBINDO PHARMA |
201168 |
002 |
ANDA |
LAMOTRIGINE |
LAMOTRIGINE |
TABLET, FOR SUSPENSION;ORAL |
25MG |
Prescription |
No |
No |
AB |
2014/06/12
|
ALEMBIC |