| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 65862-830-03 | 65862-830 | HUMAN PRESCRIPTION DRUG | Prasugrel | Prasugrel | TABLET, FILM COATED | ORAL | 20171016 | N/A | ANDA | ANDA205888 | Aurobindo Pharma Limited | PRASUGREL HYDROCHLORIDE | 10 mg/1 | 3 BLISTER PACK in 1 CARTON (65862-830-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-830-10) |
| 65862-830-30 | 65862-830 | HUMAN PRESCRIPTION DRUG | Prasugrel | Prasugrel | TABLET, FILM COATED | ORAL | 20171016 | N/A | ANDA | ANDA205888 | Aurobindo Pharma Limited | PRASUGREL HYDROCHLORIDE | 10 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-830-30) |
| 65862-829-03 | 65862-829 | HUMAN PRESCRIPTION DRUG | Prasugrel | Prasugrel | TABLET, FILM COATED | ORAL | 20171016 | N/A | ANDA | ANDA205888 | Aurobindo Pharma Limited | PRASUGREL HYDROCHLORIDE | 5 mg/1 | 3 BLISTER PACK in 1 CARTON (65862-829-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-829-10) |
| 65862-829-30 | 65862-829 | HUMAN PRESCRIPTION DRUG | Prasugrel | Prasugrel | TABLET, FILM COATED | ORAL | 20171016 | N/A | ANDA | ANDA205888 | Aurobindo Pharma Limited | PRASUGREL HYDROCHLORIDE | 5 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-829-30) |