美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=JUVISYNC
符合检索条件的记录共6
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1药品名称JUVISYNC
申请号202343产品号001
活性成分SIMVASTATIN; SITAGLIPTIN PHOSPHATE市场状态停止上市
剂型或给药途径TABLET;ORAL规格10MG;EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期2011/10/07申请机构MERCK SHARP AND DOHME CORP
2药品名称JUVISYNC
申请号202343产品号002
活性成分SIMVASTATIN; SITAGLIPTIN PHOSPHATE市场状态停止上市
剂型或给药途径TABLET;ORAL规格20MG;EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期2011/10/07申请机构MERCK SHARP AND DOHME CORP
3药品名称JUVISYNC
申请号202343产品号003
活性成分SIMVASTATIN; SITAGLIPTIN PHOSPHATE市场状态停止上市
剂型或给药途径TABLET;ORAL规格40MG;EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期2011/10/07申请机构MERCK SHARP AND DOHME CORP
4药品名称JUVISYNC
申请号202343产品号004
活性成分SIMVASTATIN; SITAGLIPTIN PHOSPHATE市场状态停止上市
剂型或给药途径TABLET;ORAL规格10MG;EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期2012/09/18申请机构MERCK SHARP AND DOHME CORP
5药品名称JUVISYNC
申请号202343产品号005
活性成分SIMVASTATIN; SITAGLIPTIN PHOSPHATE市场状态停止上市
剂型或给药途径TABLET;ORAL规格20MG;EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期2012/09/18申请机构MERCK SHARP AND DOHME CORP
6药品名称JUVISYNC
申请号202343产品号006
活性成分SIMVASTATIN; SITAGLIPTIN PHOSPHATE市场状态停止上市
剂型或给药途径TABLET;ORAL规格40MG;EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期2012/09/18申请机构MERCK SHARP AND DOHME CORP