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 |
2015/12/03 |
SUPPL-83(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2015/10/09 |
SUPPL-82(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2012/12/17 |
SUPPL-81(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2005/10/20 |
SUPPL-67(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1999/11/30 |
SUPPL-64(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1999/09/30 |
SUPPL-66(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1999/02/24 |
SUPPL-65(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1996/12/11 |
SUPPL-63(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1995/05/26 |
SUPPL-61(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1995/05/23 |
SUPPL-62(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1990/11/02 |
SUPPL-58(补充) |
Approval |
Labeling |
|
|
|
1990/09/19 |
SUPPL-59(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/10/22 |
SUPPL-56(补充) |
Approval |
Labeling |
|
|
|
1985/10/25 |
SUPPL-55(补充) |
Approval |
Labeling |
|
|
|
1985/06/19 |
SUPPL-54(补充) |
Approval |
Labeling |
|
|
|
1984/11/13 |
SUPPL-52(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1984/09/27 |
SUPPL-50(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1984/06/12 |
SUPPL-51(补充) |
Approval |
Labeling |
|
|
|
1984/03/28 |
SUPPL-46(补充) |
Approval |
Labeling |
|
|
|
1983/07/26 |
SUPPL-49(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1983/07/26 |
SUPPL-45(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1983/07/19 |
SUPPL-48(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1983/07/19 |
SUPPL-47(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1983/06/13 |
SUPPL-44(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/07/29 |
SUPPL-41(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1981/01/02 |
SUPPL-16(补充) |
Approval |
Labeling |
|
|
|
1980/05/20 |
SUPPL-37(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1979/07/18 |
SUPPL-36(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1979/07/18 |
SUPPL-33(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1978/11/06 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1978/11/06 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1978/05/26 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1977/07/01 |
SUPPL-18(补充) |
Approval |
Labeling |
|
|
|
1977/07/01 |
SUPPL-17(补充) |
Approval |
Labeling |
|
|
|
1976/06/25 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1975/05/16 |
SUPPL-10(补充) |
Approval |
Labeling |
|
|
|
1975/05/16 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1975/05/16 |
SUPPL-6(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1973/01/02 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
STANDARD
|
|
|
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:NORETHINDRONE 剂型/给药途径:TABLET;ORAL-28 规格:0.35MG 治疗等效代码:AB1
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 |
017060 |
001 |
NDA |
NOR-QD |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Prescription |
Yes |
Yes |
AB1 |
Approved Prior to Jan 1, 1982
|
TEVA BRANDED PHARM |
076177 |
001 |
ANDA |
CAMILA |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Prescription |
No |
No |
AB1 |
2002/10/21
|
DR REDDYS LABS SA |
090454 |
001 |
ANDA |
HEATHER |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Prescription |
No |
No |
AB1 |
2010/04/23
|
GLENMARK PHARMS LTD |
091325 |
001 |
ANDA |
NORETHINDRONE |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Prescription |
No |
No |
AB1 |
2011/09/19
|
LUPIN LTD |
201483 |
001 |
ANDA |
NORETHINDRONE |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Prescription |
No |
No |
AB1 |
2013/06/24
|
XIROMED |
202260 |
001 |
ANDA |
NORETHINDRONE |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Discontinued |
No |
No |
AB1 |
2013/08/01
|
AMNEAL PHARMS |
202014 |
001 |
ANDA |
NORETHINDRONE |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Prescription |
No |
No |
AB1 |
2013/09/13
|
NOVAST LABS |
207304 |
001 |
ANDA |
INCASSIA |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Prescription |
No |
No |
AB1 |
2016/09/23
|
AUROBINDO PHARMA |
206807 |
001 |
ANDA |
NORETHINDRONE |
NORETHINDRONE |
TABLET;ORAL-28 |
0.35MG |
Prescription |
No |
No |
AB1 |
2016/12/13
|
NAARI PTE LTD |