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=ANDA212781"
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
71610-518-42 71610-518 HUMAN PRESCRIPTION DRUG Ranolazine RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240401 N/A ANDA ANDA212781 Aphena Pharma Solutions - Tennessee, LLC RANOLAZINE 500 mg/1 1800 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-518-42)
71610-518-83 71610-518 HUMAN PRESCRIPTION DRUG Ranolazine RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210122 N/A ANDA ANDA212781 Aphena Pharma Solutions - Tennessee, LLC RANOLAZINE 500 mg/1 3600 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-518-83)
70625-207-02 70625-207 HUMAN PRESCRIPTION DRUG Ranolazine RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200401 N/A ANDA ANDA212781 SunGen Pharma LLC RANOLAZINE 1000 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70625-207-02)
42291-773-60 42291-773 HUMAN PRESCRIPTION DRUG Ranolazine RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20201027 N/A ANDA ANDA212781 AvKARE RANOLAZINE 500 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-773-60)
42291-774-60 42291-774 HUMAN PRESCRIPTION DRUG Ranolazine RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20201027 N/A ANDA ANDA212781 AvKARE RANOLAZINE 1000 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-774-60)
70625-207-01 70625-207 HUMAN PRESCRIPTION DRUG Ranolazine RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200401 N/A ANDA ANDA212781 SunGen Pharma LLC RANOLAZINE 1000 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70625-207-01)
70625-206-02 70625-206 HUMAN PRESCRIPTION DRUG Ranolazine RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200401 N/A ANDA ANDA212781 SunGen Pharma LLC RANOLAZINE 500 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70625-206-02)
70625-206-01 70625-206 HUMAN PRESCRIPTION DRUG Ranolazine RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200401 N/A ANDA ANDA212781 SunGen Pharma LLC RANOLAZINE 500 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70625-206-01)
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