| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 65862-691-05 | 65862-691 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20180611 | N/A | ANDA | ANDA203962 | Aurobindo Pharma Limited | SILDENAFIL CITRATE | 100 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-691-05) |
| 65862-691-30 | 65862-691 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20180611 | N/A | ANDA | ANDA203962 | Aurobindo Pharma Limited | SILDENAFIL CITRATE | 100 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-691-30) |
| 65862-690-01 | 65862-690 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20180611 | N/A | ANDA | ANDA203962 | Aurobindo Pharma Limited | SILDENAFIL CITRATE | 50 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-690-01) |