药品注册申请号:201802
申请类型:ANDA (仿制药申请)
申请人:STRIDES PHARMA
申请人全名:STRIDES PHARMA GLOBAL PTE 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 EFAVIRENZ; EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG No No AB 2023/10/03 2023/10/03 Discontinued
002 EFAVIRENZ; EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 300MG No No AB -- Prescription
003 EFAVIRENZ; EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG No No AB -- 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
2023/10/03 ORIG-1(原始申请) Approval Not Applicable
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:EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 剂型/给药途径:TABLET;ORAL 规格:600MG;200MG;300MG 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
021937 001 NDA ATRIPLA EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Discontinued Yes No AB 2006/07/12 GILEAD SCIENCES
203041 001 ANDA EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Prescription No Yes AB 2018/09/04 AUROBINDO PHARMA
091215 001 ANDA EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Prescription No No AB 2018/11/09 TEVA PHARMS USA
206894 001 ANDA EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Prescription No No AB 2019/06/03 CIPLA
204287 001 ANDA EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Prescription No No AB 2021/09/13 MACLEODS PHARMS LTD
213541 001 ANDA EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Prescription No No AB 2021/12/22 LAURUS
203053 001 ANDA EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Prescription No No AB 2022/01/24 HETERO LABS LTD V
201802 001 ANDA EFAVIRENZ; EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Discontinued No No AB 2023/10/03 STRIDES PHARMA
209061 001 ANDA EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG;200MG;300MG Discontinued No No AB 2024/09/05 MYLAN
活性成分:EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 剂型/给药途径:TABLET;ORAL 规格:300MG 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
201802 002 ANDA EFAVIRENZ; EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 300MG Prescription No No AB -- STRIDES PHARMA
活性成分:EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 剂型/给药途径:TABLET;ORAL 规格:600MG 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
201802 003 ANDA EFAVIRENZ; EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE TABLET;ORAL 600MG Prescription No No AB -- STRIDES PHARMA
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