| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 61958-3001-1 | 61958-3001 | HUMAN PRESCRIPTION DRUG | Sunlenca | LENACAPAVIR SODIUM | TABLET, FILM COATED | ORAL | 20221222 | N/A | NDA | NDA215974 | Gilead Sciences, Inc. | LENACAPAVIR SODIUM | 300 mg/1 | 1 POUCH in 1 CARTON (61958-3001-1) / 1 BLISTER PACK in 1 POUCH / 4 TABLET, FILM COATED in 1 BLISTER PACK |
| 61958-3001-2 | 61958-3001 | HUMAN PRESCRIPTION DRUG | Sunlenca | LENACAPAVIR SODIUM | TABLET, FILM COATED | ORAL | 20221222 | N/A | NDA | NDA215974 | Gilead Sciences, Inc. | LENACAPAVIR SODIUM | 300 mg/1 | 1 POUCH in 1 CARTON (61958-3001-2) / 1 BLISTER PACK in 1 POUCH / 5 TABLET, FILM COATED in 1 BLISTER PACK |
| 61958-3001-3 | 61958-3001 | HUMAN PRESCRIPTION DRUG | Sunlenca | LENACAPAVIR SODIUM | TABLET, FILM COATED | ORAL | 20241113 | N/A | NDA | NDA215974 | Gilead Sciences, Inc. | LENACAPAVIR SODIUM | 300 mg/1 | 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-3001-3) |