药品注册申请号:091198
申请类型:ANDA (仿制药申请)
申请人:SANDOZ
申请人全名:SANDOZ INC
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 DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 5MG No No AB 2011/05/10 2011/05/10 Discontinued
002 DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 10MG No No AB 2011/05/10 Discontinued
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
2019/12/19 SUPPL-9(补充) Approval Labeling STANDARD
2016/11/17 SUPPL-8(补充) Approval Labeling STANDARD
2016/11/17 SUPPL-6(补充) Approval Labeling STANDARD
2011/05/10 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:DONEPEZIL HYDROCHLORIDE 剂型/给药途径:TABLET, ORALLY DISINTEGRATING;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RLDRSTE Code产品号批准日期申请人
091198 001 ANDA DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 5MG Discontinued No No AB 2011/05/10 SANDOZ
201787 001 ANDA DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 5MG Prescription No No AB 2012/12/14 MACLEODS PHARMS LTD
205269 001 ANDA DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 5MG Prescription No No AB 2018/07/27 HISUN PHARM HANGZHOU
活性成分:DONEPEZIL HYDROCHLORIDE 剂型/给药途径:TABLET, ORALLY DISINTEGRATING;ORAL 规格:10MG 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
091198 002 ANDA DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 10MG Discontinued No No AB 2011/05/10 SANDOZ
201787 002 ANDA DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 10MG Prescription No Yes AB 2012/12/14 MACLEODS PHARMS LTD
205269 002 ANDA DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 10MG Prescription No No AB 2018/07/27 HISUN PHARM HANGZHOU
更多信息
药品NDC数据与药品包装、标签说明书
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