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=NDA016689"
符合检索条件的记录共 3 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
0338-0077-04 0338-0077 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride Dextrose and Sodium Chloride INJECTION, SOLUTION INTRAVENOUS 19701208 N/A NDA NDA016689 Baxter Healthcare Corporation DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; 200 mg/100mL 14 BAG in 1 CARTON (0338-0077-04) / 1000 mL in 1 BAG
0338-0077-03 0338-0077 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride Dextrose and Sodium Chloride INJECTION, SOLUTION INTRAVENOUS 19701208 N/A NDA NDA016689 Baxter Healthcare Corporation DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; 200 mg/100mL 24 BAG in 1 CARTON (0338-0077-03) / 500 mL in 1 BAG
0338-0077-02 0338-0077 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride Dextrose and Sodium Chloride INJECTION, SOLUTION INTRAVENOUS 19701208 N/A NDA NDA016689 Baxter Healthcare Corporation DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; 200 mg/100mL 36 BAG in 1 CARTON (0338-0077-02) / 250 mL in 1 BAG
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