| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 50090-6355-0 | 50090-6355 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | POWDER, FOR SUSPENSION | ORAL | 20230202 | N/A | ANDA | ANDA065334 | A-S Medication Solutions | AMOXICILLIN | 400 mg/5mL | 75 mL in 1 BOTTLE (50090-6355-0) |
| 65862-070-75 | 65862-070 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | POWDER, FOR SUSPENSION | ORAL | 20061228 | N/A | ANDA | ANDA065334 | Aurobindo Pharma Limited | AMOXICILLIN | 200 mg/5mL | 75 mL in 1 BOTTLE (65862-070-75) |
| 65862-071-01 | 65862-071 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | POWDER, FOR SUSPENSION | ORAL | 20061228 | N/A | ANDA | ANDA065334 | Aurobindo Pharma Limited | AMOXICILLIN | 400 mg/5mL | 100 mL in 1 BOTTLE (65862-071-01) |
| 65862-071-75 | 65862-071 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | POWDER, FOR SUSPENSION | ORAL | 20061228 | N/A | ANDA | ANDA065334 | Aurobindo Pharma Limited | AMOXICILLIN | 400 mg/5mL | 75 mL in 1 BOTTLE (65862-071-75) |
| 50090-6680-0 | 50090-6680 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | POWDER, FOR SUSPENSION | ORAL | 20230908 | N/A | ANDA | ANDA065334 | A-S Medication Solutions | AMOXICILLIN | 400 mg/5mL | 50 mL in 1 BOTTLE (50090-6680-0) |