美国药品NDC数据库(National Drug Code Database)=>当前查询条件:"申请号:ANDA207667;",共 4 条结果。点击左侧“产品NDC”可以查询指定剂量规格药品的所有包装规格及药品说明书。
产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 市场分类 申请号 标签持有者 活性成分 规格 规格单位
55150-262HUMAN PRESCRIPTION DRUGMethylprednisolone Sodium SuccinateMethylprednisolone Sodium SuccinateINJECTION, POWDER, LYOPHILIZED, FOR SOLUTIONINTRAMUSCULAR; INTRAVENOUS20151215ANDAANDA207667AuroMedics Pharma LLCMETHYLPREDNISOLONE SODIUM SUCCINATE40mg/1
55150-263HUMAN PRESCRIPTION DRUGMethylprednisolone Sodium SuccinateMethylprednisolone Sodium SuccinateINJECTION, POWDER, LYOPHILIZED, FOR SOLUTIONINTRAMUSCULAR; INTRAVENOUS20151215ANDAANDA207667AuroMedics Pharma LLCMETHYLPREDNISOLONE SODIUM SUCCINATE125mg/1
55150-264HUMAN PRESCRIPTION DRUGMethylprednisolone Sodium SuccinateMethylprednisolone Sodium SuccinateINJECTION, POWDER, LYOPHILIZED, FOR SOLUTIONINTRAMUSCULAR; INTRAVENOUS20151215ANDAANDA207667AuroMedics Pharma LLCMETHYLPREDNISOLONE SODIUM SUCCINATE500mg/1
55150-265HUMAN PRESCRIPTION DRUGMethylprednisolone Sodium SuccinateMethylprednisolone Sodium SuccinateINJECTION, POWDER, LYOPHILIZED, FOR SOLUTIONINTRAMUSCULAR; INTRAVENOUS20151215ANDAANDA207667AuroMedics Pharma LLCMETHYLPREDNISOLONE SODIUM SUCCINATE2g/1