药品注册申请号:209997
申请类型:ANDA (仿制药申请)
申请人:FRESENIUS KABI USA
申请人全名:FRESENIUS KABI USA LLC
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 SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 1.34GM/5ML;1.38GM/5ML (268MG/ML;276MG/ML) No Yes AP 2022/03/30 2022/03/30 Prescription
002 SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML) No No AP 2022/03/30 Prescription
003 SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 13.4GM/50ML;13.8GM/50ML (268MG/ML;276MG/ML) No Yes AP 2022/03/30 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
2022/03/30 ORIG-1(原始申请) Approval STANDARD
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:SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE 剂型/给药途径:SOLUTION;INTRAVENOUS 规格:1.34GM/5ML;1.38GM/5ML (268MG/ML;276MG/ML) 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
209997 001 ANDA SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 1.34GM/5ML;1.38GM/5ML (268MG/ML;276MG/ML) Prescription No Yes AP 2022/03/30 FRESENIUS KABI USA
218314 001 ANDA SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 1.34GM/5ML;1.38GM/5ML (268MG/ML;276MG/ML) Prescription No No AP 2024/06/21 AM REGENT
活性成分:SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE 剂型/给药途径:SOLUTION;INTRAVENOUS 规格:4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML) 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
018892 001 NDA SODIUM PHOSPHATES IN PLASTIC CONTAINER SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML) Prescription Yes Yes AP 1983/05/10 HOSPIRA
209997 002 ANDA SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML) Prescription No No AP 2022/03/30 FRESENIUS KABI USA
218314 002 ANDA SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML) Prescription No No AP 2024/06/21 AM REGENT
活性成分:SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE 剂型/给药途径:SOLUTION;INTRAVENOUS 规格:13.4GM/50ML;13.8GM/50ML (268MG/ML;276MG/ML) 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
209997 003 ANDA SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 13.4GM/50ML;13.8GM/50ML (268MG/ML;276MG/ML) Prescription No Yes AP 2022/03/30 FRESENIUS KABI USA
218314 003 ANDA SODIUM PHOSPHATES SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE SOLUTION;INTRAVENOUS 13.4GM/50ML;13.8GM/50ML (268MG/ML;276MG/ML) Prescription No No AP 2024/06/21 AM REGENT
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