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 157 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
51655-534-83 51655-534 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA077739 Northwind Health Company, LLC METOPROLOL TARTRATE 25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-534-83)
50090-6076-0 50090-6076 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220915 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6076-0)
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)
65862-062-99 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)
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)
43063-821-30 43063-821 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20180627 20270831 ANDA ANDA077739 PD-Rx Pharmaceuticals, Inc. METOPROLOL TARTRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-30)
43063-821-60 43063-821 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20180517 20270831 ANDA ANDA077739 PD-Rx Pharmaceuticals, Inc. METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-60)
43063-821-90 43063-821 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20170105 20270831 ANDA ANDA077739 PD-Rx Pharmaceuticals, Inc. METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-90)
43063-821-93 43063-821 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20170105 20270831 ANDA ANDA077739 PD-Rx Pharmaceuticals, Inc. METOPROLOL TARTRATE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-93)
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)
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)
70518-3293-1 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)
70518-3293-3 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)
43063-927-01 43063-927 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20191009 N/A ANDA ANDA077739 PD-Rx Pharmaceuticals, Inc. METOPROLOL TARTRATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-927-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase