药品注册申请号:075731
申请类型:ANDA (仿制药申请)
申请人:TARO
申请人全名:TARO PHARMACEUTICAL INDUSTRIES LTD
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 CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 15MG No No AB 2000/04/27 2000/04/27 Prescription
002 CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 7.5MG No No AB 2000/04/27 Prescription
003 CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 3.75MG No No AB 2000/04/27 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
2024/10/17 SUPPL-13(补充) Approval Labeling STANDARD
2024/10/17 SUPPL-12(补充) Approval Labeling STANDARD
2024/10/17 SUPPL-9(补充) Approval Labeling STANDARD
2013/03/20 SUPPL-5(补充) Approval Labeling
2011/09/27 SUPPL-3(补充) Approval Labeling
2010/01/20 SUPPL-2(补充) Approval Labeling
2000/04/27 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
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
与本品治疗等效的药品
活性成分:CLORAZEPATE DIPOTASSIUM 剂型/给药途径:TABLET;ORAL 规格:15MG 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
071858 001 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 15MG Prescription No Yes AB 1987/07/17 AUROBINDO PHARMA
075731 001 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 15MG Prescription No No AB 2000/04/27 TARO
215566 003 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 15MG Prescription No No AB 2022/06/14 COREPHARMA
213730 003 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 15MG Prescription No No AB 2022/12/16 NOVITIUM PHARMA
活性成分:CLORAZEPATE DIPOTASSIUM 剂型/给药途径:TABLET;ORAL 规格:7.5MG 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RLDRSTE Code产品号批准日期申请人
017105 007 NDA TRANXENE CLORAZEPATE DIPOTASSIUM TABLET;ORAL 7.5MG Prescription Yes No AB Approved Prior to Jan 1, 1982 AJENAT PHARMS
071858 003 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 7.5MG Prescription No No AB 1987/07/17 AUROBINDO PHARMA
075731 002 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 7.5MG Prescription No No AB 2000/04/27 TARO
215566 002 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 7.5MG Prescription No No AB 2022/06/14 COREPHARMA
213730 002 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 7.5MG Prescription No No AB 2022/06/16 NOVITIUM PHARMA
活性成分:CLORAZEPATE DIPOTASSIUM 剂型/给药途径:TABLET;ORAL 规格:3.75MG 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
071858 002 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 3.75MG Prescription No No AB 1987/07/17 AUROBINDO PHARMA
075731 003 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 3.75MG Prescription No No AB 2000/04/27 TARO
215566 001 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 3.75MG Prescription No No AB 2022/06/14 COREPHARMA
213730 001 ANDA CLORAZEPATE DIPOTASSIUM CLORAZEPATE DIPOTASSIUM TABLET;ORAL 3.75MG Prescription No No AB 2022/06/16 NOVITIUM PHARMA
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