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"
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
72789-535-90 72789-535 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20251119 N/A ANDA ANDA077739 PD-Rx Pharmaceuticals, Inc. METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-535-90)
50090-2207-0 50090-2207 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151030 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (50090-2207-0)
50090-2207-1 50090-2207 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151030 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-2207-1)
50090-2207-2 50090-2207 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151030 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-2207-2)
50090-2207-3 50090-2207 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151030 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-2207-3)
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)
51655-527-25 51655-527 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20221025 N/A ANDA ANDA077739 Northwind Health Company, LLC METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-25)
51655-527-26 51655-527 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220916 N/A ANDA ANDA077739 Northwind Health Company, LLC METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-26)
50090-2149-0 50090-2149 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151020 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-2149-0)
50090-2149-1 50090-2149 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151020 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-2149-1)
50090-2149-4 50090-2149 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151020 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-2149-4)
50090-2149-5 50090-2149 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151020 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (50090-2149-5)
71610-080-53 71610-080 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA077739 Aphena Pharma Solutions - Tennessee, LLC METOPROLOL TARTRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71610-080-53)
71610-080-60 71610-080 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA077739 Aphena Pharma Solutions - Tennessee, LLC METOPROLOL TARTRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-080-60)
71610-080-80 71610-080 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA077739 Aphena Pharma Solutions - Tennessee, LLC METOPROLOL TARTRATE 100 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-080-80)
51655-514-25 51655-514 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220714 N/A ANDA ANDA077739 Northwind Health Company, LLC METOPROLOL TARTRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-25)
51655-514-26 51655-514 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA077739 Northwind Health Company, LLC METOPROLOL TARTRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-26)
51655-514-52 51655-514 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220808 N/A ANDA ANDA077739 Northwind Health Company, LLC METOPROLOL TARTRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-52)
51655-514-83 51655-514 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20230106 N/A ANDA ANDA077739 Northwind Health Company, LLC METOPROLOL TARTRATE 100 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-83)
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