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=ANDA071135"
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
71610-459-20 71610-459 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20201007 N/A ANDA ANDA071135 Aphena Pharma Solutions - Tennessee, LLC DIAZEPAM 5 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (71610-459-20)
71610-459-15 71610-459 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20200901 N/A ANDA ANDA071135 Aphena Pharma Solutions - Tennessee, LLC DIAZEPAM 5 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (71610-459-15)
67544-019-75 67544-019 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20060327 N/A ANDA ANDA071135 Aphena Pharma Solutions - Tennessee, LLC DIAZEPAM 5 mg/1 150 TABLET in 1 BOTTLE, PLASTIC (67544-019-75)
67544-019-80 67544-019 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20060327 N/A ANDA ANDA071135 Aphena Pharma Solutions - Tennessee, LLC DIAZEPAM 5 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (67544-019-80)
67544-019-90 67544-019 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20060327 N/A ANDA ANDA071135 Aphena Pharma Solutions - Tennessee, LLC DIAZEPAM 5 mg/1 240 TABLET in 1 BOTTLE, PLASTIC (67544-019-90)
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