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=ANDA200815"
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
63629-2192-1 63629-2192 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20111215 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 10 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2192-1)
63629-2196-1 63629-2196 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20111215 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 5 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2196-1)
0603-3581-21 0603-3581 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20090331 N/A ANDA ANDA200815 Endo USA, Inc. FELODIPINE 2.5 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3581-21)
0603-3581-28 0603-3581 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20090331 N/A ANDA ANDA200815 Endo USA, Inc. FELODIPINE 2.5 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3581-28)
63629-2193-1 63629-2193 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20090331 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 2.5 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2193-1)
0603-3583-21 0603-3583 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20111215 N/A ANDA ANDA200815 Endo USA, Inc. FELODIPINE 10 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3583-21)
0603-3583-28 0603-3583 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20111215 N/A ANDA ANDA200815 Endo USA, Inc. FELODIPINE 10 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3583-28)
63629-2191-1 63629-2191 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20111215 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 10 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2191-1)
63629-2195-1 63629-2195 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20210312 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 5 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2195-1)
72162-1160-1 72162-1160 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 10 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1160-1)
72162-1160-5 72162-1160 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 10 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1160-5)
0603-3582-21 0603-3582 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20111215 N/A ANDA ANDA200815 Endo USA, Inc. FELODIPINE 5 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3582-21)
0603-3582-28 0603-3582 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20111215 N/A ANDA ANDA200815 Endo USA, Inc. FELODIPINE 5 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3582-28)
63629-2194-1 63629-2194 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20090331 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 2.5 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2194-1)
72162-1158-1 72162-1158 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 2.5 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1158-1)
72162-1158-5 72162-1158 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, EXTENDED RELEASE ORAL 20230330 N/A ANDA ANDA200815 Bryant Ranch Prepack FELODIPINE 2.5 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1158-5)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase