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
43063-970-04 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190731 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 4 TABLET in 1 BOTTLE, PLASTIC (43063-970-04)
43063-970-06 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190513 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 6 TABLET in 1 BOTTLE, PLASTIC (43063-970-06)
43063-970-10 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20200805 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (43063-970-10)
43063-970-15 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20191204 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (43063-970-15)
43063-970-21 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190507 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (43063-970-21)
43063-970-30 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190501 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-970-30)
43063-970-60 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20191126 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (43063-970-60)
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)
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)
0172-3926-70 0172-3926 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 19861210 N/A ANDA ANDA071321 Teva Pharmaceuticals USA, Inc. DIAZEPAM 5 mg/1 500 TABLET in 1 BOTTLE (0172-3926-70)
0172-3926-80 0172-3926 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 19861210 N/A ANDA ANDA071321 Teva Pharmaceuticals USA, Inc. DIAZEPAM 5 mg/1 1000 TABLET in 1 BOTTLE (0172-3926-80)
67046-0943-3 67046-0943 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20260505 N/A ANDA ANDA071321 Coupler LLC DIAZEPAM 5 mg/1 30 TABLET in 1 BLISTER PACK (67046-0943-3)
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)
71335-1584-8 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)
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