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)
产品NDC16714-120
产品类型HUMAN PRESCRIPTION DRUG
商品名Fosaprepitant
通用名Fosaprepitant
剂型INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
给药途径INTRAVENOUS
市场类别ANDA
申请号ANDA209965
标签持有者NorthStar RxLLC
活性成分FOSAPREPITANT DIMEGLUMINE
规格150 mg/5mL
药学分类Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A4 Inducers [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Neurokinin 1 Antagonists [MoA], Substance P/Neurokinin-1 Receptor Antagonist [EPC]
DEA计划编号N/A
上市认证有效期20241231
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产品NDCNDC包装代码包装描述开始上市日期结束上市日期NDC号状态是否样品包装药品说明书
16714-12016714-120-011 VIAL in 1 CARTON (16714-120-01) / 1 mL in 1 VIAL20200116有效药品说明书及标签信息
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