| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71205-509-90 | 71205-509 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20201124 | N/A | ANDA | ANDA078380 | Proficient Rx LP | SILDENAFIL CITRATE | 20 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-509-90) |
| 71205-509-60 | 71205-509 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20201124 | N/A | ANDA | ANDA078380 | Proficient Rx LP | SILDENAFIL CITRATE | 20 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-509-60) |
| 71205-509-30 | 71205-509 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20201124 | N/A | ANDA | ANDA078380 | Proficient Rx LP | SILDENAFIL CITRATE | 20 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-509-30) |