| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72303-0845-1 | 72303-0845 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20200611 | N/A | ANDA | ANDA213032 | HEC Pharm USA Inc. | SILDENAFIL CITRATE | 25 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (72303-0845-1) |
| 72303-0847-1 | 72303-0847 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20200611 | N/A | ANDA | ANDA213032 | HEC Pharm USA Inc. | SILDENAFIL CITRATE | 100 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (72303-0847-1) |
| 72303-0846-1 | 72303-0846 | HUMAN PRESCRIPTION DRUG | Sildenafil | Sildenafil | TABLET, FILM COATED | ORAL | 20200611 | N/A | ANDA | ANDA213032 | HEC Pharm USA Inc. | SILDENAFIL CITRATE | 50 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (72303-0846-1) |