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=NDA016677"
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
0338-9659-75 0338-9659 HUMAN PRESCRIPTION DRUG SODIUM CHLORIDE sodium chloride INJECTION, SOLUTION INTRAVENOUS 20240809 N/A NDA NDA016677 Baxter Healthcare Corporation SODIUM CHLORIDE 9 g/1000mL 50 mL in 1 BAG (0338-9659-75)
0338-9661-60 0338-9661 HUMAN PRESCRIPTION DRUG SODIUM CHLORIDE sodium chloride INJECTION, SOLUTION INTRAVENOUS 20240809 N/A NDA NDA016677 Baxter Healthcare Corporation SODIUM CHLORIDE 9 g/1000mL 100 mL in 1 BAG (0338-9661-60)
0338-9663-60 0338-9663 HUMAN PRESCRIPTION DRUG SODIUM CHLORIDE sodium chloride INJECTION, SOLUTION INTRAVENOUS 20240809 N/A NDA NDA016677 Baxter Healthcare Corporation SODIUM CHLORIDE 9 g/1000mL 100 mL in 1 BAG (0338-9663-60)
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