| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 59651-333-01 | 59651-333 | HUMAN PRESCRIPTION DRUG | Albuterol | Albuterol | TABLET | ORAL | 20200514 | N/A | ANDA | ANDA213657 | Aurobindo Pharma Limited | ALBUTEROL SULFATE | 2 mg/1 | 100 TABLET in 1 BOTTLE (59651-333-01) |
| 59651-333-05 | 59651-333 | HUMAN PRESCRIPTION DRUG | Albuterol | Albuterol | TABLET | ORAL | 20200514 | N/A | ANDA | ANDA213657 | Aurobindo Pharma Limited | ALBUTEROL SULFATE | 2 mg/1 | 500 TABLET in 1 BOTTLE (59651-333-05) |
| 59651-334-01 | 59651-334 | HUMAN PRESCRIPTION DRUG | Albuterol | Albuterol | TABLET | ORAL | 20200514 | N/A | ANDA | ANDA213657 | Aurobindo Pharma Limited | ALBUTEROL SULFATE | 4 mg/1 | 100 TABLET in 1 BOTTLE (59651-334-01) |
| 59651-334-05 | 59651-334 | HUMAN PRESCRIPTION DRUG | Albuterol | Albuterol | TABLET | ORAL | 20200514 | N/A | ANDA | ANDA213657 | Aurobindo Pharma Limited | ALBUTEROL SULFATE | 4 mg/1 | 500 TABLET in 1 BOTTLE (59651-334-05) |