药品注册申请号:020386
申请类型:NDA (新药申请)
申请人:ORGANON
申请人全名:ORGANON LLC A SUB OF ORGANON AND CO
产品信息
产品号商品名活性成分剂型/给药途径规格/剂量参比药物(RLD)生物等效参考标准(RS)治疗等效代码该申请号批准日期该产品号批准日期市场状态
001 COZAAR LOSARTAN POTASSIUM TABLET;ORAL 25MG Yes No AB 1995/04/14 1995/04/14 Prescription
002 COZAAR LOSARTAN POTASSIUM TABLET;ORAL 50MG Yes No AB 1995/04/14 Prescription
003 COZAAR LOSARTAN POTASSIUM TABLET;ORAL 100MG Yes Yes AB 1998/10/13 Prescription
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
2021/10/15 SUPPL-64(补充) Approval Labeling STANDARD
2018/10/12 SUPPL-62(补充) Approval Labeling STANDARD
2015/12/11 SUPPL-54(补充) Approval Labeling STANDARD
2014/09/29 SUPPL-61(补充) Approval Labeling STANDARD
2014/02/20 SUPPL-59(补充) Approval Manufacturing (CMC) STANDARD
2014/01/17 SUPPL-60(补充) Approval Labeling STANDARD
2013/03/27 SUPPL-58(补充) Approval Labeling STANDARD
2012/09/28 SUPPL-57(补充) Approval Labeling UNKNOWN
2011/11/17 SUPPL-56(补充) Approval Labeling UNKNOWN
2011/06/10 SUPPL-53(补充) Approval Labeling UNKNOWN
2010/09/23 SUPPL-52(补充) Approval Labeling UNKNOWN
2009/06/05 SUPPL-49(补充) Approval Labeling STANDARD
2006/09/21 SUPPL-46(补充) Approval Labeling STANDARD
2006/09/21 SUPPL-43(补充) Approval Labeling STANDARD
2006/08/29 SUPPL-45(补充) Approval Labeling STANDARD
2006/03/31 SUPPL-42(补充) Approval Labeling STANDARD
2005/04/12 SUPPL-40(补充) Approval Labeling STANDARD
2005/04/12 SUPPL-39(补充) Approval Labeling STANDARD
2004/03/11 SUPPL-29(补充) Approval Efficacy STANDARD
2004/03/11 SUPPL-19(补充) Approval Labeling STANDARD
2003/03/25 SUPPL-32(补充) Approval Efficacy PRIORITY
2002/10/23 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
2002/09/17 SUPPL-28(补充) Approval Efficacy PRIORITY
2002/01/10 SUPPL-27(补充) Approval Manufacturing (CMC) STANDARD
2001/10/03 SUPPL-22(补充) Approval Labeling STANDARD
2001/08/24 SUPPL-26(补充) Approval Labeling STANDARD
2001/07/03 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
2001/06/22 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
2001/05/16 SUPPL-24(补充) Approval Manufacturing (CMC) STANDARD
2000/02/23 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
2000/01/28 SUPPL-18(补充) Approval Labeling STANDARD
2000/01/19 SUPPL-20(补充) Approval Labeling STANDARD
1999/06/09 SUPPL-17(补充) Approval Labeling STANDARD
1999/05/13 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1998/11/24 SUPPL-15(补充) Approval Labeling STANDARD
1998/10/13 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1998/08/31 SUPPL-14(补充) Approval Labeling STANDARD
1998/08/31 SUPPL-13(补充) Approval Labeling STANDARD
1998/08/31 SUPPL-11(补充) Approval Labeling STANDARD
1998/04/03 SUPPL-12(补充) Approval Labeling STANDARD
1998/03/27 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1998/03/09 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1998/02/25 SUPPL-6(补充) Approval Labeling STANDARD
1997/11/07 SUPPL-7(补充) Approval Labeling STANDARD
1996/08/07 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1996/07/18 SUPPL-4(补充) Approval Labeling STANDARD
1995/12/29 SUPPL-1(补充) Approval Efficacy STANDARD
1995/12/01 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1995/11/22 SUPPL-2(补充) Approval Labeling STANDARD
1995/04/14 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity 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
001 5138069 2009/08/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5138069*PED 2010/02/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5153197 2009/10/06 U-3 PDF格式**本条是由Drugfuture回溯的历史信息**
5153197*PED 2010/04/06 U-3 PDF格式**本条是由Drugfuture回溯的历史信息**
5210079 2010/05/11 U-496 PDF格式**本条是由Drugfuture回溯的历史信息**
5210079*PED 2010/11/11 U-496 PDF格式**本条是由Drugfuture回溯的历史信息**
5608075 2014/03/04 PDF格式**本条是由Drugfuture回溯的历史信息**
5608075*PED 2014/09/04 PDF格式**本条是由Drugfuture回溯的历史信息**
002 5138069 2009/08/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5138069*PED 2010/02/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5153197 2009/10/06 U-3 PDF格式**本条是由Drugfuture回溯的历史信息**
5153197*PED 2010/04/06 U-3 PDF格式**本条是由Drugfuture回溯的历史信息**
5210079 2010/05/11 U-496 PDF格式**本条是由Drugfuture回溯的历史信息**
5210079*PED 2010/11/11 U-496 PDF格式**本条是由Drugfuture回溯的历史信息**
5608075 2014/03/04 PDF格式**本条是由Drugfuture回溯的历史信息**
5608075*PED 2014/09/04 PDF格式**本条是由Drugfuture回溯的历史信息**
003 5138069 2009/08/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5138069*PED 2010/02/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5153197 2009/10/06 U-3 PDF格式**本条是由Drugfuture回溯的历史信息**
5153197*PED 2010/04/06 U-3 PDF格式**本条是由Drugfuture回溯的历史信息**
5210079 2010/05/11 U-496 PDF格式**本条是由Drugfuture回溯的历史信息**
5210079*PED 2010/11/11 U-496 PDF格式**本条是由Drugfuture回溯的历史信息**
5608075 2014/03/04 PDF格式**本条是由Drugfuture回溯的历史信息**
5608075*PED 2014/09/04 PDF格式**本条是由Drugfuture回溯的历史信息**
与本品相关的市场独占权保护信息
关联产品号独占权代码失效日期备注
001 NPP 2007/03/11**本条是由Drugfuture回溯的历史信息**
PED 2007/09/11**本条是由Drugfuture回溯的历史信息**
002 NPP 2007/03/11**本条是由Drugfuture回溯的历史信息**
PED 2007/09/11**本条是由Drugfuture回溯的历史信息**
003 NPP 2007/03/11**本条是由Drugfuture回溯的历史信息**
PED 2007/09/11**本条是由Drugfuture回溯的历史信息**
与本品治疗等效的药品
活性成分:LOSARTAN POTASSIUM 剂型/给药途径:TABLET;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RLDRSTE Code产品号批准日期申请人
020386 001 NDA COZAAR LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription Yes No AB 1995/04/14 ORGANON
077424 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2010/10/06 CHARTWELL RX
077459 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Discontinued No No AB 2010/10/06 HIKMA
078232 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2010/10/06 LUPIN LTD
078243 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2010/10/06 ZYDUS PHARMS USA INC
090083 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2010/10/06 AUROBINDO PHARMA
090382 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2010/10/06 STRIDES PHARMA
090428 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2010/10/06 ALEMBIC PHARMS LTD
091129 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2010/10/06 WATSON LABS
091497 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2011/06/06 PRINSTON INC
202230 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2012/05/30 MACLEODS PHARMS LTD
201170 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2012/09/18 JUBILANT CADISTA
091541 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2012/09/24 MICRO LABS
200290 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2013/08/30 IPCA LABS LTD
203835 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2015/08/12 HETERO LABS LTD V
203030 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2015/10/14 UNICHEM
215959 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2023/02/23 GRANULES
217396 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2023/08/14 MSN
218551 001 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2024/06/04 APOTEX
活性成分:LOSARTAN POTASSIUM 剂型/给药途径:TABLET;ORAL 规格:50MG 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RLDRSTE Code产品号批准日期申请人
020386 002 NDA COZAAR LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription Yes No AB 1995/04/14 ORGANON
077424 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2010/10/06 CHARTWELL RX
077459 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Discontinued No No AB 2010/10/06 HIKMA
078232 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2010/10/06 LUPIN LTD
078243 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2010/10/06 ZYDUS PHARMS USA INC
090083 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2010/10/06 AUROBINDO PHARMA
090382 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2010/10/06 STRIDES PHARMA
090428 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2010/10/06 ALEMBIC PHARMS LTD
091129 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2010/10/06 WATSON LABS
091497 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2011/06/06 PRINSTON INC
202230 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2012/05/30 MACLEODS PHARMS LTD
201170 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2012/09/18 JUBILANT CADISTA
091541 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2012/09/24 MICRO LABS
200290 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2013/08/30 IPCA LABS LTD
203835 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2015/08/12 HETERO LABS LTD V
203030 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2015/10/14 UNICHEM
215959 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2023/02/23 GRANULES
217396 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2023/08/14 MSN
218551 002 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2024/06/04 APOTEX
活性成分:LOSARTAN POTASSIUM 剂型/给药途径:TABLET;ORAL 规格:100MG 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RLDRSTE Code产品号批准日期申请人
020386 003 NDA COZAAR LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription Yes Yes AB 1998/10/13 ORGANON
077424 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2010/10/06 CHARTWELL RX
077459 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Discontinued No No AB 2010/10/06 HIKMA
078232 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2010/10/06 LUPIN LTD
078243 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2010/10/06 ZYDUS PHARMS USA INC
090083 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2010/10/06 AUROBINDO PHARMA
090382 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2010/10/06 STRIDES PHARMA
090428 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2010/10/06 ALEMBIC PHARMS LTD
091129 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2010/10/06 WATSON LABS
091497 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2011/06/06 PRINSTON INC
202230 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2012/05/30 MACLEODS PHARMS LTD
201170 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2012/09/18 JUBILANT CADISTA
091541 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2012/09/24 MICRO LABS
200290 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2013/08/30 IPCA LABS LTD
203835 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2015/08/12 HETERO LABS LTD V
203030 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2015/10/14 UNICHEM
215959 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2023/02/23 GRANULES
217396 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2023/08/14 MSN
218551 003 ANDA LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET;ORAL 100MG Prescription No No AB 2024/06/04 APOTEX
更多信息
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