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=ANDA200981"
符合检索条件的记录共 223 条，共 12 页，当前第 6 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
67296-1903-6 67296-1903 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA200981 RedPharm Drug, Inc METOPROLOL TARTRATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (67296-1903-6)
67296-1903-1 67296-1903 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA200981 RedPharm Drug, Inc METOPROLOL TARTRATE 25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (67296-1903-1)
67296-1903-3 67296-1903 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA200981 RedPharm Drug, Inc METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67296-1903-3)
67296-1903-9 67296-1903 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA200981 RedPharm Drug, Inc METOPROLOL TARTRATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (67296-1903-9)
67296-2098-1 67296-2098 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA200981 RedPharm Drug METOPROLOL TARTRATE 25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (67296-2098-1)
68071-3723-3 68071-3723 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20241120 N/A ANDA ANDA200981 NuCare Pharmaceuticals, Inc. METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3723-3)
68071-3723-6 68071-3723 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20241120 N/A ANDA ANDA200981 NuCare Pharmaceuticals, Inc. METOPROLOL TARTRATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3723-6)
68071-3723-8 68071-3723 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20241210 N/A ANDA ANDA200981 NuCare Pharmaceuticals, Inc. METOPROLOL TARTRATE 25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-3723-8)
68071-4755-2 68071-4755 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20190206 N/A ANDA ANDA200981 NuCare Pharmaceuticals,Inc. METOPROLOL TARTRATE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68071-4755-2)
68071-4755-8 68071-4755 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20190206 N/A ANDA ANDA200981 NuCare Pharmaceuticals,Inc. METOPROLOL TARTRATE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-4755-8)
68071-4755-9 68071-4755 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20190206 N/A ANDA ANDA200981 NuCare Pharmaceuticals,Inc. METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-4755-9)
68071-4880-1 68071-4880 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20190502 N/A ANDA ANDA200981 NuCare Pharmaceuticals,Inc. METOPROLOL TARTRATE 100 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68071-4880-1)
68071-4880-9 68071-4880 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20190502 N/A ANDA ANDA200981 NuCare Pharmaceuticals,Inc. METOPROLOL TARTRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-4880-9)
68071-4957-1 68071-4957 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20190703 N/A ANDA ANDA200981 NuCare Pharmaceuticals,Inc. METOPROLOL TARTRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-4957-1)
68071-4958-1 68071-4958 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20190705 N/A ANDA ANDA200981 NuCare Pharmaceuticals,Inc. METOPROLOL TARTRATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-4958-1)
68071-5236-1 68071-5236 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20200403 N/A ANDA ANDA200981 NuCare Pharmaceuticals,Inc. METOPROLOL TARTRATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-5236-1)
68788-8211-1 68788-8211 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220607 N/A ANDA ANDA200981 Preferred Pharmaceuticals Inc. METOPROLOL TARTRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8211-1)
68788-8211-3 68788-8211 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220607 N/A ANDA ANDA200981 Preferred Pharmaceuticals Inc. METOPROLOL TARTRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8211-3)
68788-8211-6 68788-8211 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220607 N/A ANDA ANDA200981 Preferred Pharmaceuticals Inc. METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8211-6)
68788-8211-9 68788-8211 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220607 N/A ANDA ANDA200981 Preferred Pharmaceuticals Inc. METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8211-9)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase