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=ANDA203908"
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
65862-665-30 65862-665 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 20 mg/1 30 TABLET in 1 BOTTLE (65862-665-30)
65862-665-78 65862-665 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 20 mg/1 10 BLISTER PACK in 1 CARTON (65862-665-78) / 10 TABLET in 1 BLISTER PACK (65862-665-10)
71205-392-30 71205-392 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20200130 N/A ANDA ANDA203908 Proficient Rx LP ARIPIPRAZOLE 5 mg/1 30 TABLET in 1 BOTTLE (71205-392-30)
71205-392-60 71205-392 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20200130 N/A ANDA ANDA203908 Proficient Rx LP ARIPIPRAZOLE 5 mg/1 60 TABLET in 1 BOTTLE (71205-392-60)
71205-392-90 71205-392 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20200130 N/A ANDA ANDA203908 Proficient Rx LP ARIPIPRAZOLE 5 mg/1 90 TABLET in 1 BOTTLE (71205-392-90)
71335-1364-1 71335-1364 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20191004 N/A ANDA ANDA203908 Bryant Ranch Prepack ARIPIPRAZOLE 20 mg/1 30 TABLET in 1 BOTTLE (71335-1364-1)
71335-1364-2 71335-1364 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20191004 N/A ANDA ANDA203908 Bryant Ranch Prepack ARIPIPRAZOLE 20 mg/1 28 TABLET in 1 BOTTLE (71335-1364-2)
71335-1364-3 71335-1364 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20191004 N/A ANDA ANDA203908 Bryant Ranch Prepack ARIPIPRAZOLE 20 mg/1 90 TABLET in 1 BOTTLE (71335-1364-3)
65862-662-01 65862-662 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 5 mg/1 100 TABLET in 1 BOTTLE (65862-662-01)
65862-662-05 65862-662 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 5 mg/1 500 TABLET in 1 BOTTLE (65862-662-05)
65862-662-30 65862-662 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 5 mg/1 30 TABLET in 1 BOTTLE (65862-662-30)
65862-662-78 65862-662 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 5 mg/1 10 BLISTER PACK in 1 CARTON (65862-662-78) / 10 TABLET in 1 BLISTER PACK (65862-662-10)
65862-666-01 65862-666 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 30 mg/1 100 TABLET in 1 BOTTLE (65862-666-01)
65862-666-05 65862-666 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 30 mg/1 500 TABLET in 1 BOTTLE (65862-666-05)
65862-666-30 65862-666 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 30 mg/1 30 TABLET in 1 BOTTLE (65862-666-30)
65862-666-78 65862-666 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20151008 N/A ANDA ANDA203908 Aurobindo Pharma Limited ARIPIPRAZOLE 30 mg/1 10 BLISTER PACK in 1 CARTON (65862-666-78) / 10 TABLET in 1 BLISTER PACK (65862-666-10)
82804-023-30 82804-023 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20231011 N/A ANDA ANDA203908 Proficient Rx LP ARIPIPRAZOLE 10 mg/1 30 TABLET in 1 BOTTLE (82804-023-30)
82804-023-60 82804-023 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20231011 N/A ANDA ANDA203908 Proficient Rx LP ARIPIPRAZOLE 10 mg/1 60 TABLET in 1 BOTTLE (82804-023-60)
82804-023-90 82804-023 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20231011 N/A ANDA ANDA203908 Proficient Rx LP ARIPIPRAZOLE 10 mg/1 90 TABLET in 1 BOTTLE (82804-023-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase