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 2 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
76420-953-01 76420-953 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-953-01)
76420-953-20 76420-953 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (76420-953-20)
76420-953-30 76420-953 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-953-30)
76420-953-60 76420-953 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-953-60)
76420-953-90 76420-953 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-953-90)
68645-191-59 68645-191 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 20270731 ANDA ANDA077739 Legacy Pharmaceutical Packaging, LLC METOPROLOL TARTRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68645-191-59)
51655-534-25 51655-534 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20220302 N/A ANDA ANDA077739 Northwind Health Company, 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 Health Company, 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 Health Company, LLC METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-534-52)
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)
68645-190-59 68645-190 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 20270731 ANDA ANDA077739 Legacy Pharmaceutical Packaging, LLC METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68645-190-59)
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)
51655-527-52 51655-527 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20221021 N/A ANDA ANDA077739 Northwind Health Company, 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 Health Company, LLC METOPROLOL TARTRATE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-83)
70882-133-60 70882-133 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20070911 N/A ANDA ANDA077739 Cambridge Therapeutics Technologies, LLC METOPROLOL TARTRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (70882-133-60)
71335-0192-1 71335-0192 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20180309 N/A ANDA ANDA077739 Bryant Ranch Prepack METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0192-1)
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