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 7 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
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)
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)
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)
76420-054-00 76420-054 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-054-00)
76420-054-01 76420-054 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-054-01)
76420-054-20 76420-054 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20201024 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 25 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (76420-054-20)
76420-054-30 76420-054 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20201024 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-054-30)
76420-054-60 76420-054 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-054-60)
76420-054-90 76420-054 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA077739 Asclemed USA, Inc. METOPROLOL TARTRATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-054-90)
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)
55154-4752-0 55154-4752 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET, FILM COATED ORAL 20100513 N/A ANDA ANDA077739 Cardinal Health 107, LLC METOPROLOL TARTRATE 25 mg/1 10 BLISTER PACK in 1 BAG (55154-4752-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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)
63187-609-60 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 60 TABLET, FILM COATED in 1 BOTTLE (63187-609-60)
63187-609-72 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/1 120 TABLET, FILM COATED in 1 BOTTLE (63187-609-72)
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