美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）
检索条件:" 注册申请号=NDA019691"
符合检索条件的记录共 2 条，共 1 页，当前第 1 页 ，可点击列名称排序
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
0990-7109-09 0990-7109 HUMAN PRESCRIPTION DRUG Potassium Chloride in Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20200125 N/A NDA NDA019691 ICU Medical Inc. DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE 50 g/1000mL; 2.98 g/1000mL; 9 g/1000mL 12 POUCH in 1 CASE (0990-7109-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG
0990-7107-09 0990-7107 HUMAN PRESCRIPTION DRUG Potassium Chloride in Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20200201 N/A NDA NDA019691 ICU Medical Inc. DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE 50 g/1000mL; 1.49 g/1000mL; 9 g/1000mL 12 POUCH in 1 CASE (0990-7107-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG
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