| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 59651-775-01 | 59651-775 | HUMAN PRESCRIPTION DRUG | SOTALOL HYDROCHLORIDE | SOTALOL HYDROCHLORIDE | TABLET | ORAL | 20230629 | N/A | ANDA | ANDA077616 | Aurobindo Pharma Limited | SOTALOL HYDROCHLORIDE | 80 mg/1 | 100 TABLET in 1 BOTTLE (59651-775-01) |
| 59651-777-01 | 59651-777 | HUMAN PRESCRIPTION DRUG | SOTALOL HYDROCHLORIDE | SOTALOL HYDROCHLORIDE | TABLET | ORAL | 20230629 | N/A | ANDA | ANDA077616 | Aurobindo Pharma Limited | SOTALOL HYDROCHLORIDE | 160 mg/1 | 100 TABLET in 1 BOTTLE (59651-777-01) |
| 59651-776-01 | 59651-776 | HUMAN PRESCRIPTION DRUG | SOTALOL HYDROCHLORIDE | SOTALOL HYDROCHLORIDE | TABLET | ORAL | 20230629 | N/A | ANDA | ANDA077616 | Aurobindo Pharma Limited | SOTALOL HYDROCHLORIDE | 120 mg/1 | 100 TABLET in 1 BOTTLE (59651-776-01) |