| 101 | 药品名称 | POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER | ||
| 申请号 | 019367 | 产品号 | 007 | |
| 活性成分 | CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE | 市场状态 | 处方药 | |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML | |
| 治疗等效代码 | AP | 参比药物 | 否 | |
| 批准日期 | 1985/04/05 | 申请机构 | BAXTER HEALTHCARE CORP | |
| 102 | 药品名称 | POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER | ||
| 申请号 | 019367 | 产品号 | 008 | |
| 活性成分 | CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE | 市场状态 | 处方药 | |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML | |
| 治疗等效代码 | AP | 参比药物 | 否 | |
| 批准日期 | 1985/04/05 | 申请机构 | BAXTER HEALTHCARE CORP | |
| 103 | 药品名称 | POTASSIUM CHLORIDE | ||
| 申请号 | 019439 | 产品号 | 001 | |
| 活性成分 | POTASSIUM CHLORIDE | 市场状态 | 停止上市 | |
| 剂型或给药途径 | TABLET, EXTENDED RELEASE;ORAL | 规格 | 20MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | |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 | 1986/06/13 | 申请机构 | MERCK INC | |
| 104 | 药品名称 | POTASSIUM CHLORIDE | ||
| 申请号 | 019439 | 产品号 | 002 | |
| 活性成分 | POTASSIUM CHLORIDE | 市场状态 | 停止上市 | |
| 剂型或给药途径 | TABLET, EXTENDED RELEASE;ORAL | 规格 | 10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | |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 | 1986/06/13 | 申请机构 | MERCK INC | |
| 105 | 药品名称 | POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER | ||
| 申请号 | 019630 | 产品号 | 001 | |
| 活性成分 | DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE | 市场状态 | 处方药 | |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 5GM/100ML;37MG/100ML;110MG/100ML | |
| 治疗等效代码 | 参比药物 | 否 | ||
| 批准日期 | 1988/02/17 | 申请机构 | B BRAUN MEDICAL INC | |
| 106 | 药品名称 | POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER | ||
| 申请号 | 019630 | 产品号 | 002 | |
| 活性成分 | DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE | 市场状态 | 处方药 | |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 5GM/100ML;75MG/100ML;110MG/100ML | |
| 治疗等效代码 | 参比药物 | 否 | ||
| 批准日期 | 1988/02/17 | 申请机构 | B BRAUN MEDICAL INC | |
| 107 | 药品名称 | POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER | ||
| 申请号 | 019630 | 产品号 | 003 | |
| 活性成分 | DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE | 市场状态 | 处方药 | |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 5GM/100ML;110MG/100ML;110MG/100ML | |
| 治疗等效代码 | 参比药物 | 否 | ||
| 批准日期 | 1988/02/17 | 申请机构 | B BRAUN MEDICAL INC | |
| 108 | 药品名称 | POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER | ||
| 申请号 | 019630 | 产品号 | 004 | |
| 活性成分 | DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE | 市场状态 | 处方药 | |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 5GM/100ML;150MG/100ML;110MG/100ML | |
| 治疗等效代码 | 参比药物 | 否 | ||
| 批准日期 | 1988/02/17 | 申请机构 | B BRAUN MEDICAL INC | |
| 109 | 药品名称 | POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER | ||
| 申请号 | 019630 | 产品号 | 005 | |
| 活性成分 | DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE | 市场状态 | 处方药 | |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 5GM/100ML;220MG/100ML;110MG/100ML | |
| 治疗等效代码 | 参比药物 | 否 | ||
| 批准日期 | 1988/02/17 | 申请机构 | B BRAUN MEDICAL INC | |
| 110 | 药品名称 | POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER | ||
| 申请号 | 019630 | 产品号 | 006 | |
| 活性成分 | DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE | 市场状态 | 处方药 | |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 5GM/100ML;300MG/100ML;110MG/100ML | |
| 治疗等效代码 | 参比药物 | 否 | ||
| 批准日期 | 1988/02/17 | 申请机构 | B BRAUN MEDICAL INC | |
©2006-2024 DrugFuture->U.S. FDA Drugs Database
|