| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 59572-740-14 | 59572-740 | HUMAN PRESCRIPTION DRUG | ONUREG | azacitidine | TABLET, FILM COATED | ORAL | 20200901 | N/A | NDA | NDA214120 | Celgene Corporation | AZACITIDINE | 300 mg/1 | 14 TABLET, FILM COATED in 1 BOTTLE (59572-740-14) |
| 59572-740-07 | 59572-740 | HUMAN PRESCRIPTION DRUG | ONUREG | azacitidine | TABLET, FILM COATED | ORAL | 20201218 | N/A | NDA | NDA214120 | Celgene Corporation | AZACITIDINE | 300 mg/1 | 7 TABLET, FILM COATED in 1 BLISTER PACK (59572-740-07) |
| 59572-730-14 | 59572-730 | HUMAN PRESCRIPTION DRUG | ONUREG | azacitidine | TABLET, FILM COATED | ORAL | 20200901 | N/A | NDA | NDA214120 | Celgene Corporation | AZACITIDINE | 200 mg/1 | 14 TABLET, FILM COATED in 1 BOTTLE (59572-730-14) |
| 59572-730-07 | 59572-730 | HUMAN PRESCRIPTION DRUG | ONUREG | azacitidine | TABLET, FILM COATED | ORAL | 20201218 | N/A | NDA | NDA214120 | Celgene Corporation | AZACITIDINE | 200 mg/1 | 7 TABLET, FILM COATED in 1 BLISTER PACK (59572-730-07) |