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=ANDA207667"
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
55150-264-20 55150-264 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20151215 N/A ANDA ANDA207667 AuroMedics Pharma LLC METHYLPREDNISOLONE SODIUM SUCCINATE 500 mg/1 1 VIAL, MULTI-DOSE in 1 CARTON (55150-264-20) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, MULTI-DOSE
55150-262-03 55150-262 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20151215 N/A ANDA ANDA207667 AuroMedics Pharma LLC METHYLPREDNISOLONE SODIUM SUCCINATE 40 mg/1 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-262-03) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
55150-265-50 55150-265 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20151215 N/A ANDA ANDA207667 AuroMedics Pharma LLC METHYLPREDNISOLONE SODIUM SUCCINATE 2 g/1 1 VIAL, SINGLE-DOSE in 1 CARTON (55150-265-50) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
55150-263-03 55150-263 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20151215 N/A ANDA ANDA207667 AuroMedics Pharma LLC METHYLPREDNISOLONE SODIUM SUCCINATE 125 mg/1 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-263-03) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase