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=ANDA211211"
符合检索条件的记录共 4 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
17271-735-06 17271-735 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE and SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20250515 N/A ANDA ANDA211211 BECTON DICKINSON AND COMPANY DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; .9 g/100mL 20 BAG in 1 CASE (17271-735-06) / 500 mL in 1 BAG
17271-735-07 17271-735 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE and SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20250515 N/A ANDA ANDA211211 BECTON DICKINSON AND COMPANY DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; .9 g/100mL 10 BAG in 1 CASE (17271-735-07) / 1000 mL in 1 BAG
63323-870-10 63323-870 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE and SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20201026 N/A ANDA ANDA211211 Fresenius Kabi USA, LLC DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; .9 g/100mL 20 BAG in 1 CASE (63323-870-10) / 500 mL in 1 BAG (63323-870-01)
63323-870-74 63323-870 HUMAN PRESCRIPTION DRUG Dextrose and Sodium Chloride DEXTROSE MONOHYDRATE and SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20201026 N/A ANDA ANDA211211 Fresenius Kabi USA, LLC DEXTROSE MONOHYDRATE; SODIUM CHLORIDE 5 g/100mL; .9 g/100mL 10 BAG in 1 CASE (63323-870-74) / 1000 mL in 1 BAG (63323-870-04)
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