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=ANDA216916"
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
70010-781-01 70010-781 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 50 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-01)
70010-781-05 70010-781 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 50 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-05)
70010-781-10 70010-781 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 50 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-10)
70010-782-01 70010-782 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 100 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-01)
70010-782-05 70010-782 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 100 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-05)
70010-782-10 70010-782 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 100 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-10)
70010-783-01 70010-783 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 200 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-783-01)
70010-783-05 70010-783 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 200 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-783-05)
70010-783-10 70010-783 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 200 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-783-10)
70010-780-10 70010-780 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 25 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-10)
70010-780-05 70010-780 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 25 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-05)
70010-780-01 70010-780 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231002 N/A ANDA ANDA216916 Granules Pharmaceuticals Inc. METOPROLOL SUCCINATE 25 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-01)
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