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=ANDA071321"
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
71335-1584-0 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 120 TABLET in 1 BOTTLE (71335-1584-0)
71335-1584-1 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 12 TABLET in 1 BOTTLE (71335-1584-1)
71335-1584-2 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 15 TABLET in 1 BOTTLE (71335-1584-2)
71335-1584-3 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 20 TABLET in 1 BOTTLE (71335-1584-3)
71335-1584-4 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 30 TABLET in 1 BOTTLE (71335-1584-4)
71335-1584-5 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 60 TABLET in 1 BOTTLE (71335-1584-5)
71335-1584-6 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 90 TABLET in 1 BOTTLE (71335-1584-6)
71335-1584-7 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 10 TABLET in 1 BOTTLE (71335-1584-7)
71335-1584-8 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 2 TABLET in 1 BOTTLE (71335-1584-8)
71335-1584-9 71335-1584 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20220210 N/A ANDA ANDA071321 Bryant Ranch Prepack DIAZEPAM 5 mg/1 1 TABLET in 1 BOTTLE (71335-1584-9)
70518-1713-0 70518-1713 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20181206 N/A ANDA ANDA071321 REMEDYREPACK INC. DIAZEPAM 5 mg/1 30 TABLET in 1 BLISTER PACK (70518-1713-0)
0172-3926-60 0172-3926 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 19861210 N/A ANDA ANDA071321 Teva Pharmaceuticals USA, Inc. DIAZEPAM 5 mg/1 100 TABLET in 1 BOTTLE (0172-3926-60)
50090-1913-1 50090-1913 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20150702 N/A ANDA ANDA071321 A-S Medication Solutions DIAZEPAM 5 mg/1 20 TABLET in 1 BOTTLE (50090-1913-1)
50090-1913-2 50090-1913 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20150702 N/A ANDA ANDA071321 A-S Medication Solutions DIAZEPAM 5 mg/1 30 TABLET in 1 BOTTLE (50090-1913-2)
50090-1913-4 50090-1913 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20150702 N/A ANDA ANDA071321 A-S Medication Solutions DIAZEPAM 5 mg/1 10 TABLET in 1 BOTTLE (50090-1913-4)
50090-1913-5 50090-1913 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20150702 N/A ANDA ANDA071321 A-S Medication Solutions DIAZEPAM 5 mg/1 100 TABLET in 1 BOTTLE (50090-1913-5)
63187-173-01 63187-173 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20211021 N/A ANDA ANDA071321 Proficient Rx LP DIAZEPAM 5 mg/1 1 TABLET in 1 BOTTLE (63187-173-01)
63187-173-02 63187-173 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20180201 N/A ANDA ANDA071321 Proficient Rx LP DIAZEPAM 5 mg/1 2 TABLET in 1 BOTTLE (63187-173-02)
63187-173-10 63187-173 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20160101 N/A ANDA ANDA071321 Proficient Rx LP DIAZEPAM 5 mg/1 10 TABLET in 1 BOTTLE (63187-173-10)
63187-173-15 63187-173 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20150901 N/A ANDA ANDA071321 Proficient Rx LP DIAZEPAM 5 mg/1 15 TABLET in 1 BOTTLE (63187-173-15)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase