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=ANDA208412"
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
71205-755-12 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 12 TABLET in 1 BOTTLE (71205-755-12)
71205-755-14 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 14 TABLET in 1 BOTTLE (71205-755-14)
71205-755-15 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 15 TABLET in 1 BOTTLE (71205-755-15)
71205-755-18 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 18 TABLET in 1 BOTTLE (71205-755-18)
71205-755-20 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 20 TABLET in 1 BOTTLE (71205-755-20)
71205-755-21 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 21 TABLET in 1 BOTTLE (71205-755-21)
71205-755-24 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 24 TABLET in 1 BOTTLE (71205-755-24)
71205-755-28 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 28 TABLET in 1 BOTTLE (71205-755-28)
71205-755-30 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 30 TABLET in 1 BOTTLE (71205-755-30)
71205-755-60 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 60 TABLET in 1 BOTTLE (71205-755-60)
71205-755-90 71205-755 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20230131 N/A ANDA ANDA208412 Proficient Rx LP PREDNISONE 50 mg/1 90 TABLET in 1 BOTTLE (71205-755-90)
72189-430-05 72189-430 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230303 N/A ANDA ANDA208412 Direct_Rx PREDNISONE 20 mg/1 5 TABLET in 1 BOTTLE (72189-430-05)
72189-430-10 72189-430 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230303 N/A ANDA ANDA208412 Direct_Rx PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (72189-430-10)
72189-430-15 72189-430 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230303 N/A ANDA ANDA208412 Direct_Rx PREDNISONE 20 mg/1 15 TABLET in 1 BOTTLE (72189-430-15)
72189-430-20 72189-430 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230303 N/A ANDA ANDA208412 Direct_Rx PREDNISONE 20 mg/1 20 TABLET in 1 BOTTLE (72189-430-20)
72189-430-21 72189-430 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230303 N/A ANDA ANDA208412 Direct_Rx PREDNISONE 20 mg/1 21 TABLET in 1 BOTTLE (72189-430-21)
50090-7218-0 50090-7218 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20240813 N/A ANDA ANDA208412 A-S Medication Solutions PREDNISONE 10 mg/1 10 TABLET in 1 BOTTLE (50090-7218-0)
50090-7218-1 50090-7218 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20240813 N/A ANDA ANDA208412 A-S Medication Solutions PREDNISONE 10 mg/1 15 TABLET in 1 BOTTLE (50090-7218-1)
50090-7218-2 50090-7218 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20240813 N/A ANDA ANDA208412 A-S Medication Solutions PREDNISONE 10 mg/1 21 TABLET in 1 BOTTLE (50090-7218-2)
50090-7218-4 50090-7218 HUMAN PRESCRIPTION DRUG prednisone PREDNISONE TABLET ORAL 20240813 N/A ANDA ANDA208412 A-S Medication Solutions PREDNISONE 10 mg/1 50 TABLET in 1 BOTTLE (50090-7218-4)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase