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=NDA209939"
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
0006-3075-02 0006-3075 HUMAN PRESCRIPTION DRUG PREVYMIS LETERMOVIR TABLET, FILM COATED ORAL 20171108 N/A NDA NDA209939 Merck Sharp & Dohme LLC LETERMOVIR 240 mg/1 4 DOSE PACK in 1 CARTON (0006-3075-02) / 7 TABLET, FILM COATED in 1 DOSE PACK (0006-3075-01)
0006-3075-04 0006-3075 HUMAN PRESCRIPTION DRUG PREVYMIS LETERMOVIR TABLET, FILM COATED ORAL 20171108 N/A NDA NDA209939 Merck Sharp & Dohme LLC LETERMOVIR 240 mg/1 14 BLISTER PACK in 1 CARTON (0006-3075-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0006-3075-03)
0006-3076-02 0006-3076 HUMAN PRESCRIPTION DRUG PREVYMIS LETERMOVIR TABLET, FILM COATED ORAL 20171108 N/A NDA NDA209939 Merck Sharp & Dohme LLC LETERMOVIR 480 mg/1 4 DOSE PACK in 1 CARTON (0006-3076-02) / 7 TABLET, FILM COATED in 1 DOSE PACK (0006-3076-01)
0006-3076-04 0006-3076 HUMAN PRESCRIPTION DRUG PREVYMIS LETERMOVIR TABLET, FILM COATED ORAL 20171108 N/A NDA NDA209939 Merck Sharp & Dohme LLC LETERMOVIR 480 mg/1 14 BLISTER PACK in 1 CARTON (0006-3076-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0006-3076-03)
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