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=ANDA040489"
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
69584-611-09 69584-611 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Oxford Pharmaceuticals, LLC METHOCARBAMOL 500 mg/1 90 TABLET in 1 BOTTLE (69584-611-09)
69584-611-10 69584-611 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Oxford Pharmaceuticals, LLC METHOCARBAMOL 500 mg/1 100 TABLET in 1 BOTTLE (69584-611-10)
69584-611-50 69584-611 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Oxford Pharmaceuticals, LLC METHOCARBAMOL 500 mg/1 500 TABLET in 1 BOTTLE (69584-611-50)
69584-611-90 69584-611 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Oxford Pharmaceuticals, LLC METHOCARBAMOL 500 mg/1 1000 TABLET in 1 BOTTLE (69584-611-90)
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