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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
82868-028-06 | 82868-028 | HUMAN PRESCRIPTION DRUG | Tadalafil | Tadalafil | TABLET | ORAL | 20231121 | N/A | ANDA | ANDA206286 | Northwind Pharmaceuticals, LLC | TADALAFIL | 20 mg/1 | 6 TABLET in 1 BOTTLE, PLASTIC (82868-028-06) |
82868-028-15 | 82868-028 | HUMAN PRESCRIPTION DRUG | Tadalafil | Tadalafil | TABLET | ORAL | 20231116 | N/A | ANDA | ANDA206286 | Northwind Pharmaceuticals, LLC | TADALAFIL | 20 mg/1 | 15 TABLET in 1 BOTTLE, PLASTIC (82868-028-15) |
65862-880-60 | 65862-880 | HUMAN PRESCRIPTION DRUG | Tadalafil | Tadalafil | TABLET | ORAL | 20190205 | N/A | ANDA | ANDA206286 | Aurobindo Pharma Limited | TADALAFIL | 20 mg/1 | 60 TABLET in 1 BOTTLE (65862-880-60) |