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=ANDA207058"
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
16714-842-01 16714-842 HUMAN PRESCRIPTION DRUG Dofetilide Dofetilide CAPSULE ORAL 20180618 20240630 ANDA ANDA207058 Northstar Rx LLC DOFETILIDE .5 mg/1 60 CAPSULE in 1 BOTTLE, PLASTIC (16714-842-01)
0904-6683-08 0904-6683 HUMAN PRESCRIPTION DRUG Dofetilide Dofetilide CAPSULE ORAL 20160607 N/A ANDA ANDA207058 Major Pharmaceuticals DOFETILIDE .5 mg/1 40 BLISTER PACK in 1 CARTON (0904-6683-08) / 1 CAPSULE in 1 BLISTER PACK
16714-841-01 16714-841 HUMAN PRESCRIPTION DRUG Dofetilide Dofetilide CAPSULE ORAL 20180618 20240630 ANDA ANDA207058 Northstar Rx LLC DOFETILIDE .25 mg/1 60 CAPSULE in 1 BOTTLE, PLASTIC (16714-841-01)
0904-6682-08 0904-6682 HUMAN PRESCRIPTION DRUG Dofetilide Dofetilide CAPSULE ORAL 20160607 N/A ANDA ANDA207058 Major Pharmaceuticals DOFETILIDE .25 mg/1 40 BLISTER PACK in 1 CARTON (0904-6682-08) / 1 CAPSULE in 1 BLISTER PACK
0904-6681-08 0904-6681 HUMAN PRESCRIPTION DRUG Dofetilide Dofetilide CAPSULE ORAL 20160607 N/A ANDA ANDA207058 Major Pharmaceuticals DOFETILIDE .125 mg/1 40 BLISTER PACK in 1 CARTON (0904-6681-08) / 1 CAPSULE in 1 BLISTER PACK
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