药品注册申请号:091398
申请类型:ANDA (仿制药申请)
申请人:LUPIN LTD
申请人全名:LUPIN 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 BLISOVI 24 FE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG No No AB 2015/10/28 2015/10/28 Prescription
批准历史,通知信,药品说明书,综述等审批信息
批准日期申请类型申请提交号审查批准结论申请内容分类审评分类(优先审评;罕用药状态)通知信、综述、标签、说明书备注
2019/11/15 SUPPL 14 Approval Manufacturing (CMC) UNKNOWN
2019/05/01 SUPPL 9 Approval Manufacturing (CMC)
2019/05/01 SUPPL 5 Approval Labeling STANDARD
2019/05/01 SUPPL 1 Approval Labeling STANDARD
2015/10/28 ORIG 1 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:ETHINYL ESTRADIOL; NORETHINDRONE ACETATE 剂型/给药途径:TABLET;ORAL 规格:0.02MG;1MG 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
021871 001 NDA LOESTRIN 24 FE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG Prescription Yes No AB 2006/02/17 TEVA BRANDED PHARM
078267 001 ANDA NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG Prescription No Yes AB 2009/09/01 AMNEAL PHARMS
090293 001 ANDA GILDESS 24 FE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG Prescription No No AB 2014/12/01 VINTAGE PHARMS
090938 001 ANDA NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG Prescription No No AB 2014/12/01 BARR LABS INC
202994 001 ANDA LARIN 24 FE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG Prescription No No AB 2015/02/18 NOVAST LABS
091398 001 ANDA BLISOVI 24 FE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG Prescription No No AB 2015/10/28 LUPIN LTD
207504 001 ANDA AUROVELA 24 FE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG Prescription No No AB 2017/06/15 AUROBINDO PHARMA LTD
204847 001 ANDA NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE ETHINYL ESTRADIOL; NORETHINDRONE ACETATE TABLET;ORAL 0.02MG;1MG Prescription No No AB 2017/11/17 GLENMARK PHARMS LTD
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