药品注册申请号:216729
申请类型:ANDA (仿制药申请)
申请人:ONESOURCE SPECIALTY
申请人全名:ONESOURCE SPECIALTY 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 LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 100MCG/VIAL No No AP 2025/03/05 2025/03/05 Prescription
002 LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 200MCG/VIAL No No AP 2025/03/05 Prescription
003 LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 500MCG/VIAL No No AP 2025/03/05 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
>>>原始批准或临时批准<<<
审批日期提交号审批结论提交分类审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
2025/03/05 ORIG-1(原始申请) Approval STANDARD
>>>补充申请<<<
审批日期提交号审批结论补充类别或审批类型审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
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:LEVOTHYROXINE SODIUM; 剂型/给药途径:POWDER;INTRAVENOUS; 规格:100MCG/VIAL; 治疗等效代码:AP<<<
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
202231 001 NDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 100MCG/VIAL Prescription Yes Yes AP 2011/06/24 FRESENIUS KABI USA
206163 001 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 100MCG/VIAL Prescription No No AP 2016/06/29 PIRAMAL CRITICAL
208749 001 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 100MCG/VIAL Prescription No No AP 2018/12/21 MAIA PHARMS INC
217066 001 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 100MCG/VIAL Prescription No No AP 2023/03/24 ZYDUS PHARMS
217495 001 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 100MCG/VIAL Prescription No No AP 2024/11/29 XIROMED
216729 001 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 100MCG/VIAL Prescription No No AP 2025/03/05 ONESOURCE SPECIALTY
>>>活性成分:LEVOTHYROXINE SODIUM; 剂型/给药途径:POWDER;INTRAVENOUS; 规格:200MCG/VIAL; 治疗等效代码:AP<<<
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
202231 002 NDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 200MCG/VIAL Prescription Yes Yes AP 2011/06/24 FRESENIUS KABI USA
208749 002 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 200MCG/VIAL Prescription No No AP 2018/12/21 MAIA PHARMS INC
217066 002 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 200MCG/VIAL Prescription No No AP 2023/03/24 ZYDUS PHARMS
216729 002 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 200MCG/VIAL Prescription No No AP 2025/03/05 ONESOURCE SPECIALTY
>>>活性成分:LEVOTHYROXINE SODIUM; 剂型/给药途径:POWDER;INTRAVENOUS; 规格:500MCG/VIAL; 治疗等效代码:AP<<<
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
202231 003 NDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 500MCG/VIAL Prescription Yes Yes AP 2011/06/24 FRESENIUS KABI USA
206163 002 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 500MCG/VIAL Prescription No No AP 2016/06/29 PIRAMAL CRITICAL
208749 003 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 500MCG/VIAL Prescription No No AP 2018/12/21 MAIA PHARMS INC
217066 003 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 500MCG/VIAL Prescription No No AP 2023/03/24 ZYDUS PHARMS
216729 003 ANDA LEVOTHYROXINE SODIUM LEVOTHYROXINE SODIUM POWDER;INTRAVENOUS 500MCG/VIAL Prescription No No AP 2025/03/05 ONESOURCE SPECIALTY
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