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=ANDA078889"
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
72603-145-01 72603-145 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230410 N/A ANDA ANDA078889 Northstar Rx LLC METOPROLOL SUCCINATE 200 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-145-01)
72603-145-02 72603-145 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230410 N/A ANDA ANDA078889 Northstar Rx LLC METOPROLOL SUCCINATE 200 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-145-02)
70518-2080-1 70518-2080 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, EXTENDED RELEASE ORAL 20230119 N/A ANDA ANDA078889 REMEDYREPACK INC. METOPROLOL SUCCINATE 100 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2080-1)
68001-120-00 68001-120 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, EXTENDED RELEASE ORAL 20131125 N/A ANDA ANDA078889 BluePoint Laboratories METOPROLOL SUCCINATE 200 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-120-00)
68001-120-03 68001-120 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, EXTENDED RELEASE ORAL 20131125 N/A ANDA ANDA078889 BluePoint Laboratories METOPROLOL SUCCINATE 200 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-120-03)
68788-8255-9 68788-8255 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, EXTENDED RELEASE ORAL 20220902 N/A ANDA ANDA078889 Preferred Pharmaceuticals Inc. METOPROLOL SUCCINATE 100 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8255-9)
71335-0167-1 71335-0167 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180212 N/A ANDA ANDA078889 Bryant Ranch Prepack METOPROLOL SUCCINATE 100 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-1)
71335-0167-2 71335-0167 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180216 N/A ANDA ANDA078889 Bryant Ranch Prepack METOPROLOL SUCCINATE 100 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-2)
71335-0167-3 71335-0167 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180214 N/A ANDA ANDA078889 Bryant Ranch Prepack METOPROLOL SUCCINATE 100 mg/1 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-3)
71335-0167-4 71335-0167 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220502 N/A ANDA ANDA078889 Bryant Ranch Prepack METOPROLOL SUCCINATE 100 mg/1 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-4)
71335-0167-5 71335-0167 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220502 N/A ANDA ANDA078889 Bryant Ranch Prepack METOPROLOL SUCCINATE 100 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-5)
71335-0167-6 71335-0167 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220502 N/A ANDA ANDA078889 Bryant Ranch Prepack METOPROLOL SUCCINATE 100 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-6)
71335-0167-7 71335-0167 HUMAN PRESCRIPTION DRUG Metoprolol succinate Metoprolol succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220502 N/A ANDA ANDA078889 Bryant Ranch Prepack METOPROLOL SUCCINATE 100 mg/1 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-7)
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