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=ANDA077580"
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
70518-1182-0 70518-1182 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20180514 N/A ANDA ANDA077580 REMEDYREPACK INC. HALOPERIDOL 5 mg/1 30 TABLET in 1 BLISTER PACK (70518-1182-0)
70518-1269-0 70518-1269 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20180619 N/A ANDA ANDA077580 REMEDYREPACK INC. HALOPERIDOL 5 mg/1 30 TABLET in 1 BLISTER PACK (70518-1269-0)
70518-1599-0 70518-1599 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20181026 N/A ANDA ANDA077580 REMEDYREPACK INC. HALOPERIDOL 10 mg/1 30 TABLET in 1 BLISTER PACK (70518-1599-0)
55154-3566-0 55154-3566 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Cardinal Health 107, LLC HALOPERIDOL 5 mg/1 10 BLISTER PACK in 1 BAG (55154-3566-0) / 1 TABLET in 1 BLISTER PACK
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