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=ANDA070848"
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
82804-063-90 82804-063 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20240130 N/A ANDA ANDA070848 Proficient Rx LP SUCRALFATE 1 g/1 90 TABLET in 1 BOTTLE (82804-063-90)
68071-1749-1 68071-1749 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20200424 N/A ANDA ANDA070848 NuCare Pharmaceuticals,Inc. SUCRALFATE 1 g/1 100 TABLET in 1 BOTTLE (68071-1749-1)
0093-2210-01 0093-2210 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 19961111 N/A ANDA ANDA070848 Teva Pharmaceuticals USA, Inc. SUCRALFATE 1 g/1 100 TABLET in 1 BOTTLE (0093-2210-01)
0093-2210-05 0093-2210 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 19961111 N/A ANDA ANDA070848 Teva Pharmaceuticals USA, Inc. SUCRALFATE 1 g/1 500 TABLET in 1 BOTTLE (0093-2210-05)
0093-2210-98 0093-2210 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20110112 N/A ANDA ANDA070848 Teva Pharmaceuticals USA, Inc. SUCRALFATE 1 g/1 90 TABLET in 1 BOTTLE (0093-2210-98)
48433-091-20 48433-091 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20260313 N/A ANDA ANDA070848 Safecor Health LLC SUCRALFATE 1 g/1 100 BLISTER PACK in 1 CARTON (48433-091-20) / 1 TABLET in 1 BLISTER PACK (48433-091-01)
55154-4379-0 55154-4379 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20130924 N/A ANDA ANDA070848 Cardinal Health 107, LLC SUCRALFATE 1 g/1 10 BLISTER PACK in 1 BAG (55154-4379-0) / 1 TABLET in 1 BLISTER PACK
0615-4517-39 0615-4517 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20100108 N/A ANDA ANDA070848 NCS HealthCare of KY, LLC dba Vangard Labs SUCRALFATE 1 g/1 30 TABLET in 1 BLISTER PACK (0615-4517-39)
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