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=ANDA212875"
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
72162-2134-6 72162-2134 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20230920 N/A ANDA ANDA212875 Bryant Ranch Prepack CHLORTHALIDONE 50 mg/1 60 TABLET in 1 BOTTLE (72162-2134-6)
72162-2134-3 72162-2134 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20230920 N/A ANDA ANDA212875 Bryant Ranch Prepack CHLORTHALIDONE 50 mg/1 30 TABLET in 1 BOTTLE (72162-2134-3)
72162-2134-1 72162-2134 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20230920 N/A ANDA ANDA212875 Bryant Ranch Prepack CHLORTHALIDONE 50 mg/1 100 TABLET in 1 BOTTLE (72162-2134-1)
51224-118-70 51224-118 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20220805 N/A ANDA ANDA212875 TAGI Pharma, Inc. CHLORTHALIDONE 50 mg/1 1000 TABLET in 1 BOTTLE (51224-118-70)
51224-118-50 51224-118 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20220805 N/A ANDA ANDA212875 TAGI Pharma, Inc. CHLORTHALIDONE 50 mg/1 100 TABLET in 1 BOTTLE (51224-118-50)
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