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=ANDA040362"
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
63187-807-10 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (63187-807-10)
63187-807-12 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 12 TABLET in 1 BOTTLE (63187-807-12)
63187-807-14 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20181101 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 14 TABLET in 1 BOTTLE (63187-807-14)
63187-807-15 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 15 TABLET in 1 BOTTLE (63187-807-15)
63187-807-18 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180301 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 18 TABLET in 1 BOTTLE (63187-807-18)
63187-807-20 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 20 TABLET in 1 BOTTLE (63187-807-20)
63187-807-21 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 21 TABLET in 1 BOTTLE (63187-807-21)
63187-807-24 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 24 TABLET in 1 BOTTLE (63187-807-24)
63187-807-30 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 30 TABLET in 1 BOTTLE (63187-807-30)
63187-807-40 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 40 TABLET in 1 BOTTLE (63187-807-40)
63187-807-42 63187-807 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170201 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 20 mg/1 42 TABLET in 1 BOTTLE (63187-807-42)
61919-108-10 61919-108 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20190807 N/A ANDA ANDA040362 Direct_Rx PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (61919-108-10)
61919-108-12 61919-108 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20190807 N/A ANDA ANDA040362 Direct_Rx PREDNISONE 20 mg/1 12 TABLET in 1 BOTTLE (61919-108-12)
61919-108-14 61919-108 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20190807 N/A ANDA ANDA040362 Direct_Rx PREDNISONE 20 mg/1 14 TABLET in 1 BOTTLE (61919-108-14)
61919-108-15 61919-108 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20190807 N/A ANDA ANDA040362 Direct_Rx PREDNISONE 20 mg/1 15 TABLET in 1 BOTTLE (61919-108-15)
61919-108-20 61919-108 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20190807 N/A ANDA ANDA040362 Direct_Rx PREDNISONE 20 mg/1 20 TABLET in 1 BOTTLE (61919-108-20)
61919-235-21 61919-235 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20140101 N/A ANDA ANDA040362 DIRECT RX PREDNISONE 10 mg/1 21 TABLET in 1 BOTTLE (61919-235-21)
61919-235-30 61919-235 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20140101 N/A ANDA ANDA040362 DIRECT RX PREDNISONE 10 mg/1 30 TABLET in 1 BOTTLE (61919-235-30)
61919-235-42 61919-235 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20190807 N/A ANDA ANDA040362 Direct_Rx PREDNISONE 10 mg/1 42 TABLET in 1 BOTTLE (61919-235-42)
61919-235-10 61919-235 HUMAN PRESCRIPTION DRUG PREDNISONE PREDNISONE TABLET ORAL 20190807 N/A ANDA ANDA040362 Direct_Rx PREDNISONE 10 mg/1 10 TABLET in 1 BOTTLE (61919-235-10)
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