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 5 页 ，可点击列名称排序
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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
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)
50090-2260-0 50090-2260 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151209 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-2260-0)
50090-2260-1 50090-2260 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151209 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-2260-1)
50090-2260-3 50090-2260 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151209 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-2260-3)
50090-2260-4 50090-2260 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20151209 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 100 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (50090-2260-4)
50090-5060-0 50090-5060 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20200526 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5060-0)
50090-5070-0 50090-5070 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20200601 N/A ANDA ANDA077739 A-S Medication Solutions METOPROLOL TARTRATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5070-0)
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)
51655-514-26 51655-514 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA077739 Northwind Pharmaceuticals, 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 Pharmaceuticals, 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 Pharmaceuticals, LLC METOPROLOL TARTRATE 100 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-83)
51655-514-25 51655-514 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220714 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-25)
51655-527-25 51655-527 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20221025 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-25)
51655-534-25 51655-534 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220302 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-534-25)
51655-534-26 51655-534 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220919 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-534-26)
51655-534-52 51655-534 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220519 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-534-52)
51655-534-83 51655-534 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-534-83)
51655-527-26 51655-527 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220916 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-26)
51655-527-52 51655-527 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20221021 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-52)
51655-527-83 51655-527 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20230328 N/A ANDA ANDA077739 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-83)
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