| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 60505-4642-3 | 60505-4642 | HUMAN PRESCRIPTION DRUG | Prasugrel | Prasugrel | TABLET, FILM COATED | ORAL | 20171016 | N/A | ANDA | ANDA205897 | Apotex Corp. | PRASUGREL HYDROCHLORIDE | 5 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4642-3) |
| 60505-4643-3 | 60505-4643 | HUMAN PRESCRIPTION DRUG | Prasugrel | Prasugrel | TABLET, FILM COATED | ORAL | 20171016 | N/A | ANDA | ANDA205897 | Apotex Corp. | PRASUGREL HYDROCHLORIDE | 10 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4643-3) |
| 43817-240-01 | 43817-240 | HUMAN PRESCRIPTION DRUG | Prasugrel | Prasugrel | TABLET, FILM COATED | ORAL | 20171016 | N/A | ANDA | ANDA205897 | Panacea Biotec Limited | PRASUGREL HYDROCHLORIDE | 10 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (43817-240-01) |
| 43817-239-01 | 43817-239 | HUMAN PRESCRIPTION DRUG | Prasugrel | Prasugrel | TABLET, FILM COATED | ORAL | 20171016 | N/A | ANDA | ANDA205897 | Panacea Biotec Limited | PRASUGREL HYDROCHLORIDE | 5 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (43817-239-01) |