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=ANDA207204"
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
65162-250-09 65162-250 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20190701 N/A ANDA ANDA207204 Amneal Pharmaceuticals LLC CHLORTHALIDONE 50 mg/1 90 TABLET in 1 BOTTLE (65162-250-09)
65162-250-03 65162-250 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20190701 N/A ANDA ANDA207204 Amneal Pharmaceuticals LLC CHLORTHALIDONE 50 mg/1 30 TABLET in 1 BOTTLE (65162-250-03)
65162-247-09 65162-247 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20190701 N/A ANDA ANDA207204 Amneal Pharmaceuticals LLC CHLORTHALIDONE 25 mg/1 90 TABLET in 1 BOTTLE (65162-247-09)
65162-247-03 65162-247 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20190701 N/A ANDA ANDA207204 Amneal Pharmaceuticals LLC CHLORTHALIDONE 25 mg/1 30 TABLET in 1 BOTTLE (65162-247-03)
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