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=ANDA077739"
符合检索条件的记录共 149 条，共 8 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
63187-609-90 63187-609 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA077739 Proficient Rx LP METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-609-90)
63187-600-60 63187-600 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151201 N/A ANDA ANDA077739 Proficient Rx LP METOPROLOL TARTRATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-600-60)
63187-600-78 63187-600 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20160701 N/A ANDA ANDA077739 Proficient Rx LP METOPROLOL TARTRATE 25 mg/1 78 TABLET, FILM COATED in 1 BOTTLE (63187-600-78)
63187-600-90 63187-600 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151201 N/A ANDA ANDA077739 Proficient Rx LP METOPROLOL TARTRATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-600-90)
65862-062-01 65862-062 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Aurobindo Pharma Limited METOPROLOL TARTRATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-062-01)
65862-063-99 65862-063 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Aurobindo Pharma Limited METOPROLOL TARTRATE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-063-99)
65862-064-01 65862-064 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Aurobindo Pharma Limited METOPROLOL TARTRATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-064-01)
65862-064-60 65862-064 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Aurobindo Pharma Limited METOPROLOL TARTRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-064-60)
65862-064-99 65862-064 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Aurobindo Pharma Limited METOPROLOL TARTRATE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-064-99)
65862-062-99 65862-062 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Aurobindo Pharma Limited METOPROLOL TARTRATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-062-99)
65862-063-01 65862-063 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Aurobindo Pharma Limited METOPROLOL TARTRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-063-01)
65862-063-60 65862-063 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Aurobindo Pharma Limited METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-063-60)
67296-1424-3 67296-1424 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20210215 N/A ANDA ANDA077739 RedPharm Drug, Inc. METOPROLOL TARTRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67296-1424-3)
70518-2615-0 70518-2615 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20200309 N/A ANDA ANDA077739 REMEDYREPACK INC. METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2615-0)
70518-2615-1 70518-2615 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20240930 N/A ANDA ANDA077739 REMEDYREPACK INC. METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2615-1)
70518-3291-1 70518-3291 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20230720 N/A ANDA ANDA077739 REMEDYREPACK INC. METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3291-1)
70518-3293-3 70518-3293 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220217 N/A ANDA ANDA077739 REMEDYREPACK INC. METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3293-3)
70518-3293-1 70518-3293 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20211230 N/A ANDA ANDA077739 REMEDYREPACK INC. METOPROLOL TARTRATE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3293-1)
70518-3293-2 70518-3293 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220203 N/A ANDA ANDA077739 REMEDYREPACK INC. METOPROLOL TARTRATE 50 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3293-2)
70518-3291-0 70518-3291 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20211213 N/A ANDA ANDA077739 REMEDYREPACK INC. METOPROLOL TARTRATE 25 mg/1 60 TABLET, FILM COATED in 1 BLISTER PACK (70518-3291-0)
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