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=ANDA213412"
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
67877-696-01 67877-696 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20200213 N/A ANDA ANDA213412 Ascend Laboratories, LLC CHLORTHALIDONE 25 mg/1 100 TABLET in 1 BOTTLE (67877-696-01)
63629-8761-1 63629-8761 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20200213 N/A ANDA ANDA213412 Bryant Ranch Prepack CHLORTHALIDONE 25 mg/1 100 TABLET in 1 BOTTLE (63629-8761-1)
63629-8762-1 63629-8762 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20200213 N/A ANDA ANDA213412 Bryant Ranch Prepack CHLORTHALIDONE 50 mg/1 100 TABLET in 1 BOTTLE (63629-8762-1)
50090-6126-1 50090-6126 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20220930 N/A ANDA ANDA213412 A-S Medication Solutions CHLORTHALIDONE 25 mg/1 30 TABLET in 1 BOTTLE (50090-6126-1)
50090-6126-2 50090-6126 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20220930 N/A ANDA ANDA213412 A-S Medication Solutions CHLORTHALIDONE 25 mg/1 90 TABLET in 1 BOTTLE (50090-6126-2)
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