共 1 页 当前第 1 页 返回检索页| 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| 剂型或给药途径 | TABLET;ORAL | 规格 | 10MG;EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 否 |
| 批准日期 | 2011/10/07 | 申请机构 | MERCK SHARP AND DOHME CORP
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| 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| 剂型或给药途径 | TABLET;ORAL | 规格 | 20MG;EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 否 |
| 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| 剂型或给药途径 | TABLET;ORAL | 规格 | 40MG;EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 否 |
| 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| 剂型或给药途径 | TABLET;ORAL | 规格 | 10MG;EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 否 |
| 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| 剂型或给药途径 | TABLET;ORAL | 规格 | 20MG;EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 否 |
| 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| 剂型或给药途径 | TABLET;ORAL | 规格 | 40MG;EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 否 |
| 批准日期 | 2012/09/18 | 申请机构 | MERCK SHARP AND DOHME CORP
|