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) |