药品注册申请号:019316
申请类型:NDA (新药申请)
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 MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 5GM/10ML (500MG/ML) Yes Yes AP 1986/09/08 1986/09/08 Prescription
002 MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 1GM/2ML (500MG/ML) Yes Yes None 1986/09/08 Prescription
003 MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 10GM/20ML (500MG/ML) Yes Yes AP 2016/01/29 Prescription
004 MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 25GM/50ML (500MG/ML) Yes Yes None 2016/01/29 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
2018/03/05 SUPPL-24(补充) Approval Labeling STANDARD
2016/02/29 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
2016/01/29 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
2015/06/19 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
2013/05/29 SUPPL-18(补充) Approval Labeling UNKNOWN
2006/12/05 SUPPL-11(补充) Approval Labeling STANDARD
2000/03/01 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1998/10/28 SUPPL-8(补充) Approval Labeling STANDARD
1996/02/07 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1995/02/28 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1994/12/12 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1991/09/16 SUPPL-3(补充) Approval Labeling
1987/11/13 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1987/06/19 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1986/09/08 ORIG-1(原始申请) Approval Type 5 - New Formulation or New Manufacturer 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:MAGNESIUM SULFATE 剂型/给药途径:SOLUTION;INTRAMUSCULAR, INTRAVENOUS 规格:5GM/10ML (500MG/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
019316 001 NDA MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 5GM/10ML (500MG/ML) Prescription Yes Yes AP 1986/09/08 FRESENIUS KABI USA
075151 001 ANDA MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 5GM/10ML (500MG/ML) Prescription No Yes AP 2000/04/25 HOSPIRA
206039 001 ANDA MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 5GM/10ML (500MG/ML) Discontinued No No AP 2014/12/18 EXELA PHARMA
活性成分:MAGNESIUM SULFATE 剂型/给药途径:SOLUTION;INTRAMUSCULAR, INTRAVENOUS 规格:10GM/20ML (500MG/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
202411 001 ANDA MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 10GM/20ML (500MG/ML) Prescription No No AP 2015/05/14 HOSPIRA
019316 003 NDA MAGNESIUM SULFATE MAGNESIUM SULFATE SOLUTION;INTRAMUSCULAR, INTRAVENOUS 10GM/20ML (500MG/ML) Prescription Yes Yes AP 2016/01/29 FRESENIUS KABI USA
更多信息
药品NDC数据与药品包装、标签说明书
©2006-2024 DrugFuture->U.S. FDA Drugs Database