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=NDA016694"
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
0338-0023-02 0338-0023 HUMAN PRESCRIPTION DRUG DEXTROSE DEXTROSE MONOHYDRATE INJECTION, SOLUTION INTRAVENOUS 19710125 N/A NDA NDA016694 Baxter Healthcare Corporation DEXTROSE MONOHYDRATE 100 g/1000mL 250 mL in 1 BAG (0338-0023-02)
0338-0023-03 0338-0023 HUMAN PRESCRIPTION DRUG DEXTROSE DEXTROSE MONOHYDRATE INJECTION, SOLUTION INTRAVENOUS 19710125 N/A NDA NDA016694 Baxter Healthcare Corporation DEXTROSE MONOHYDRATE 100 g/1000mL 500 mL in 1 BAG (0338-0023-03)
0338-0023-04 0338-0023 HUMAN PRESCRIPTION DRUG DEXTROSE DEXTROSE MONOHYDRATE INJECTION, SOLUTION INTRAVENOUS 19710125 N/A NDA NDA016694 Baxter Healthcare Corporation DEXTROSE MONOHYDRATE 100 g/1000mL 1000 mL in 1 BAG (0338-0023-04)
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