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=NDA017606"
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
0990-7924-09 0990-7924 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE and SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20191201 N/A NDA NDA017606 ICU Medical Inc. DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; .225 g/100mL 12 POUCH in 1 CASE (0990-7924-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG
0990-7924-03 0990-7924 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE and SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20191201 N/A NDA NDA017606 ICU Medical Inc. DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; .225 g/100mL 24 POUCH in 1 CASE (0990-7924-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG
0990-7924-02 0990-7924 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE and SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20190901 N/A NDA NDA017606 ICU Medical Inc. DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; .225 g/100mL 24 POUCH in 1 CASE (0990-7924-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG
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