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=ANDA217843"
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
59651-652-01 59651-652 HUMAN PRESCRIPTION DRUG DIAZEPAM DIAZEPAM TABLET ORAL 20231214 N/A ANDA ANDA217843 Aurobindo Pharma Limited DIAZEPAM 2 mg/1 100 TABLET in 1 BOTTLE (59651-652-01)
59651-652-05 59651-652 HUMAN PRESCRIPTION DRUG DIAZEPAM DIAZEPAM TABLET ORAL 20231214 N/A ANDA ANDA217843 Aurobindo Pharma Limited DIAZEPAM 2 mg/1 500 TABLET in 1 BOTTLE (59651-652-05)
59651-653-01 59651-653 HUMAN PRESCRIPTION DRUG DIAZEPAM DIAZEPAM TABLET ORAL 20231214 N/A ANDA ANDA217843 Aurobindo Pharma Limited DIAZEPAM 5 mg/1 100 TABLET in 1 BOTTLE (59651-653-01)
59651-653-05 59651-653 HUMAN PRESCRIPTION DRUG DIAZEPAM DIAZEPAM TABLET ORAL 20231214 N/A ANDA ANDA217843 Aurobindo Pharma Limited DIAZEPAM 5 mg/1 500 TABLET in 1 BOTTLE (59651-653-05)
59651-653-99 59651-653 HUMAN PRESCRIPTION DRUG DIAZEPAM DIAZEPAM TABLET ORAL 20231214 N/A ANDA ANDA217843 Aurobindo Pharma Limited DIAZEPAM 5 mg/1 1000 TABLET in 1 BOTTLE (59651-653-99)
59651-654-01 59651-654 HUMAN PRESCRIPTION DRUG DIAZEPAM DIAZEPAM TABLET ORAL 20231214 N/A ANDA ANDA217843 Aurobindo Pharma Limited DIAZEPAM 10 mg/1 100 TABLET in 1 BOTTLE (59651-654-01)
59651-654-05 59651-654 HUMAN PRESCRIPTION DRUG DIAZEPAM DIAZEPAM TABLET ORAL 20231214 N/A ANDA ANDA217843 Aurobindo Pharma Limited DIAZEPAM 10 mg/1 500 TABLET in 1 BOTTLE (59651-654-05)
59651-654-99 59651-654 HUMAN PRESCRIPTION DRUG DIAZEPAM DIAZEPAM TABLET ORAL 20231214 N/A ANDA ANDA217843 Aurobindo Pharma Limited DIAZEPAM 10 mg/1 1000 TABLET in 1 BOTTLE (59651-654-99)
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