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=ANDA211861"
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
63629-1114-1 63629-1114 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20200730 N/A ANDA ANDA211861 Bryant Ranch Prepack AMPHETAMINE SULFATE 10 mg/1 100 TABLET in 1 BOTTLE (63629-1114-1)
63629-1115-1 63629-1115 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20200730 N/A ANDA ANDA211861 Bryant Ranch Prepack AMPHETAMINE SULFATE 5 mg/1 100 TABLET in 1 BOTTLE (63629-1115-1)
43547-457-10 43547-457 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20200402 N/A ANDA ANDA211861 Solco Healthcare US, LLC AMPHETAMINE SULFATE 5 mg/1 100 TABLET in 1 BOTTLE (43547-457-10)
43547-458-10 43547-458 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20200402 N/A ANDA ANDA211861 Solco Healthcare US, LLC AMPHETAMINE SULFATE 10 mg/1 100 TABLET in 1 BOTTLE (43547-458-10)
72162-1368-1 72162-1368 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20240125 N/A ANDA ANDA211861 Bryant Ranch Prepack AMPHETAMINE SULFATE 5 mg/1 100 TABLET in 1 BOTTLE (72162-1368-1)
72162-1369-1 72162-1369 HUMAN PRESCRIPTION DRUG AMPHETAMINE SULFATE amphetamine sulfate TABLET ORAL 20240125 N/A ANDA ANDA211861 Bryant Ranch Prepack AMPHETAMINE SULFATE 10 mg/1 100 TABLET in 1 BOTTLE (72162-1369-1)
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