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=ANDA218789"
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
59651-790-99 59651-790 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 1 mg/1 1000 TABLET in 1 BOTTLE (59651-790-99)
59651-791-01 59651-791 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 2 mg/1 100 TABLET in 1 BOTTLE (59651-791-01)
59651-791-99 59651-791 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 2 mg/1 1000 TABLET in 1 BOTTLE (59651-791-99)
59651-792-01 59651-792 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 5 mg/1 100 TABLET in 1 BOTTLE (59651-792-01)
59651-792-99 59651-792 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 5 mg/1 1000 TABLET in 1 BOTTLE (59651-792-99)
59651-793-01 59651-793 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 10 mg/1 100 TABLET in 1 BOTTLE (59651-793-01)
59651-793-99 59651-793 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 10 mg/1 1000 TABLET in 1 BOTTLE (59651-793-99)
59651-794-01 59651-794 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 20 mg/1 100 TABLET in 1 BOTTLE (59651-794-01)
59651-794-99 59651-794 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 20 mg/1 1000 TABLET in 1 BOTTLE (59651-794-99)
59651-790-01 59651-790 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL 1 mg/1 100 TABLET in 1 BOTTLE (59651-790-01)
59651-789-99 59651-789 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL .5 mg/1 1000 TABLET in 1 BOTTLE (59651-789-99)
59651-789-01 59651-789 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20240419 N/A ANDA ANDA218789 Aurobindo Pharma Limited HALOPERIDOL .5 mg/1 100 TABLET in 1 BOTTLE (59651-789-01)
67046-1603-3 67046-1603 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20251001 N/A ANDA ANDA218789 Coupler LLC HALOPERIDOL 5 mg/1 30 TABLET in 1 BLISTER PACK (67046-1603-3)
67046-1498-3 67046-1498 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20250128 N/A ANDA ANDA218789 Coupler LLC HALOPERIDOL 2 mg/1 30 TABLET in 1 BLISTER PACK (67046-1498-3)
71335-2937-1 71335-2937 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20251028 N/A ANDA ANDA218789 Bryant Ranch Prepack HALOPERIDOL 2 mg/1 30 TABLET in 1 BOTTLE (71335-2937-1)
67046-1548-3 67046-1548 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20250409 N/A ANDA ANDA218789 Coupler LLC HALOPERIDOL 1 mg/1 30 TABLET in 1 BLISTER PACK (67046-1548-3)
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