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=ANDA204179"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
65162-724-50 65162-724 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole TABLET, DELAYED RELEASE ORAL 20151001 N/A ANDA ANDA204179 Amneal Pharmaceuticals LLC RABEPRAZOLE SODIUM 20 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-50)
65162-724-11 65162-724 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole TABLET, DELAYED RELEASE ORAL 20151001 N/A ANDA ANDA204179 Amneal Pharmaceuticals LLC RABEPRAZOLE SODIUM 20 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-11)
65162-724-09 65162-724 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole TABLET, DELAYED RELEASE ORAL 20151001 N/A ANDA ANDA204179 Amneal Pharmaceuticals LLC RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-09)
65162-724-03 65162-724 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole TABLET, DELAYED RELEASE ORAL 20151001 N/A ANDA ANDA204179 Amneal Pharmaceuticals LLC RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-03)
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