美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=COLYTE
符合检索条件的记录共8
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1药品名称COLYTE
申请号018983产品号004
活性成分POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS市场状态停止上市
剂型或给药途径FOR SOLUTION;ORAL规格227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET
治疗等效代码参比药物
批准日期1984/10/26申请机构MEDA PHARMACEUTICALS INC
2药品名称COLYTE
申请号018983产品号005
活性成分POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS市场状态停止上市
剂型或给药途径FOR SOLUTION;ORAL规格120GM/PACKET;1.49GM/PACKET;3.36GM/PACKET;2.92GM/PACKET;11.36GM/PACKET
治疗等效代码参比药物
批准日期1984/10/26申请机构MEDA PHARMACEUTICALS INC
3药品名称COLYTE
申请号018983产品号006
活性成分POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS市场状态停止上市
剂型或给药途径FOR SOLUTION;ORAL规格360GM/PACKET;4.47GM/PACKET;10.08GM/PACKET;8.76GM/PACKET;34.08GM/PACKET
治疗等效代码参比药物
批准日期1984/10/26申请机构MEDA PHARMACEUTICALS INC
4药品名称COLYTE
申请号018983产品号007
活性成分POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS市场状态停止上市
剂型或给药途径FOR SOLUTION;ORAL规格240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT
治疗等效代码参比药物
批准日期1987/06/12申请机构MEDA PHARMACEUTICALS INC
5药品名称COLYTE-FLAVORED
申请号018983产品号008
活性成分POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS市场状态停止上市
剂型或给药途径FOR SOLUTION;ORAL规格227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT
治疗等效代码参比药物
批准日期1991/11/14申请机构MEDA PHARMACEUTICALS INC
6药品名称COLYTE-FLAVORED
申请号018983产品号009
活性成分POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS市场状态停止上市
剂型或给药途径FOR SOLUTION;ORAL规格240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT
治疗等效代码参比药物
批准日期1991/11/14申请机构MEDA PHARMACEUTICALS INC
7药品名称COLYTE
申请号018983产品号010
活性成分POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS市场状态停止上市
剂型或给药途径FOR SOLUTION;ORAL规格227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT
治疗等效代码参比药物
批准日期1989/01/31申请机构MEDA PHARMACEUTICALS INC
8药品名称COLYTE WITH FLAVOR PACKS
申请号018983产品号012
活性成分POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS市场状态处方药
剂型或给药途径FOR SOLUTION;ORAL规格240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT
治疗等效代码AA参比药物
批准日期1998/10/08申请机构MEDA PHARMACEUTICALS INC