| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 76420-497-05 | 76420-497 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20221010 | N/A | ANDA | ANDA205101 | Asclemed USA, Inc. | GABAPENTIN | 800 mg/1 | 500 TABLET in 1 BOTTLE (76420-497-05) |
| 76420-497-12 | 76420-497 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20221010 | N/A | ANDA | ANDA205101 | Asclemed USA, Inc. | GABAPENTIN | 800 mg/1 | 120 TABLET in 1 BOTTLE (76420-497-12) |
| 76420-497-24 | 76420-497 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20221010 | N/A | ANDA | ANDA205101 | Asclemed USA, Inc. | GABAPENTIN | 800 mg/1 | 240 TABLET in 1 BOTTLE (76420-497-24) |
| 82804-015-30 | 82804-015 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20231003 | N/A | ANDA | ANDA205101 | Proficient Rx LP | GABAPENTIN | 600 mg/1 | 30 TABLET in 1 BOTTLE (82804-015-30) |
| 82804-015-60 | 82804-015 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20231003 | N/A | ANDA | ANDA205101 | Proficient Rx LP | GABAPENTIN | 600 mg/1 | 60 TABLET in 1 BOTTLE (82804-015-60) |
| 82804-015-90 | 82804-015 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20231003 | N/A | ANDA | ANDA205101 | Proficient Rx LP | GABAPENTIN | 600 mg/1 | 90 TABLET in 1 BOTTLE (82804-015-90) |