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=ANDA073037"
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
60687-799-17 60687-799 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol SOLUTION ORAL 20240226 N/A ANDA ANDA073037 American Health Packaging HALOPERIDOL 2 mg/mL 10 TRAY in 1 CASE (60687-799-17) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-799-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-799-40)
0121-0581-04 0121-0581 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol SOLUTION ORAL 20091110 N/A ANDA ANDA073037 PAI Holdings, LLC dba PAI Pharma HALOPERIDOL 2 mg/mL 120 mL in 1 BOTTLE (0121-0581-04)
0121-0581-05 0121-0581 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol SOLUTION ORAL 20091110 N/A ANDA ANDA073037 PAI Holdings, LLC dba PAI Pharma HALOPERIDOL 2 mg/mL 10 TRAY in 1 CASE (0121-0581-05) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE
0121-0581-15 0121-0581 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol SOLUTION ORAL 20200612 N/A ANDA ANDA073037 PAI Holdings, LLC dba PAI Pharma HALOPERIDOL 2 mg/mL 15 mL in 1 BOTTLE (0121-0581-15)
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