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=ANDA064125"
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
25021-119-20 25021-119 HUMAN PRESCRIPTION DRUG Cefuroxime sodium Cefuroxime sodium INJECTION, POWDER, FOR SOLUTION INTRAVENOUS 20160901 N/A ANDA ANDA064125 Sagent Pharmaceuticals CEFUROXIME SODIUM 1.5 g/16mL 25 VIAL in 1 CARTON (25021-119-20) / 16 mL in 1 VIAL
25021-183-67 25021-183 HUMAN PRESCRIPTION DRUG Cefuroxime sodium Cefuroxime sodium INJECTION, POWDER, FOR SOLUTION INTRAVENOUS 20160901 N/A ANDA ANDA064125 Sagent Pharmaceuticals CEFUROXIME SODIUM 1.5 g/16mL 25 VIAL in 1 CARTON (25021-183-67) / 16 mL in 1 VIAL
25021-182-66 25021-182 HUMAN PRESCRIPTION DRUG Cefuroxime sodium Cefuroxime sodium INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20160901 N/A ANDA ANDA064125 Sagent Pharmaceuticals CEFUROXIME SODIUM 750 mg/1 25 VIAL in 1 CARTON (25021-182-66) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
25021-118-10 25021-118 HUMAN PRESCRIPTION DRUG Cefuroxime sodium Cefuroxime sodium INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20160901 N/A ANDA ANDA064125 Sagent Pharmaceuticals CEFUROXIME SODIUM 750 mg/1 25 VIAL in 1 CARTON (25021-118-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
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