| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 57962-014-28 | 57962-014 | HUMAN PRESCRIPTION DRUG | Imbruvica | Ibrutinib | TABLET, FILM COATED | ORAL | 20180216 | N/A | NDA | NDA210563 | Pharmacyclics LLC | IBRUTINIB | 140 mg/1 | 1 BLISTER PACK in 1 CARTON (57962-014-28) / 28 TABLET, FILM COATED in 1 BLISTER PACK |
| 57962-280-28 | 57962-280 | HUMAN PRESCRIPTION DRUG | Imbruvica | Ibrutinib | TABLET, FILM COATED | ORAL | 20180216 | N/A | NDA | NDA210563 | Pharmacyclics LLC | IBRUTINIB | 280 mg/1 | 1 BLISTER PACK in 1 CARTON (57962-280-28) / 28 TABLET, FILM COATED in 1 BLISTER PACK |
| 57962-420-28 | 57962-420 | HUMAN PRESCRIPTION DRUG | Imbruvica | Ibrutinib | TABLET, FILM COATED | ORAL | 20180216 | N/A | NDA | NDA210563 | Pharmacyclics LLC | IBRUTINIB | 420 mg/1 | 1 BLISTER PACK in 1 CARTON (57962-420-28) / 28 TABLET, FILM COATED in 1 BLISTER PACK |
| 57962-560-28 | 57962-560 | HUMAN PRESCRIPTION DRUG | Imbruvica | Ibrutinib | TABLET, FILM COATED | ORAL | 20180216 | 20250228 | NDA | NDA210563 | Pharmacyclics LLC | IBRUTINIB | 560 mg/1 | 1 BLISTER PACK in 1 CARTON (57962-560-28) / 28 TABLET, FILM COATED in 1 BLISTER PACK |