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=ANDA065072"
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
0143-9933-25 0143-9933 HUMAN PRESCRIPTION DRUG Cefotaxime Cefotaxime INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20021120 N/A ANDA ANDA065072 Hikma Pharmaceuticals USA Inc. CEFOTAXIME SODIUM 2 g/1 25 VIAL in 1 PACKAGE (0143-9933-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9933-01)
0143-9931-25 0143-9931 HUMAN PRESCRIPTION DRUG Cefotaxime Cefotaxime INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20021120 N/A ANDA ANDA065072 Hikma Pharmaceuticals USA Inc. CEFOTAXIME SODIUM 1 g/1 25 VIAL in 1 PACKAGE (0143-9931-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9931-01)
0143-9930-10 0143-9930 HUMAN PRESCRIPTION DRUG Cefotaxime Cefotaxime INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20021120 N/A ANDA ANDA065072 Hikma Pharmaceuticals USA Inc. CEFOTAXIME SODIUM 500 mg/1 10 VIAL in 1 PACKAGE (0143-9930-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9930-01)
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