| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1041-5 | 71335-1041 | HUMAN PRESCRIPTION DRUG | Gabapentin | GABAPENTIN | TABLET, FILM COATED | ORAL | 20190408 | N/A | ANDA | ANDA203244 | Bryant Ranch Prepack | GABAPENTIN | 800 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1041-5) |
| 71335-1041-6 | 71335-1041 | HUMAN PRESCRIPTION DRUG | Gabapentin | GABAPENTIN | TABLET, FILM COATED | ORAL | 20181227 | N/A | ANDA | ANDA203244 | Bryant Ranch Prepack | GABAPENTIN | 800 mg/1 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1041-6) |
| 71205-457-60 | 71205-457 | HUMAN PRESCRIPTION DRUG | Gabapentin | GABAPENTIN | TABLET, FILM COATED | ORAL | 20200623 | N/A | ANDA | ANDA203244 | Proficient Rx LP | GABAPENTIN | 600 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-457-60) |
| 71205-457-90 | 71205-457 | HUMAN PRESCRIPTION DRUG | Gabapentin | GABAPENTIN | TABLET, FILM COATED | ORAL | 20200623 | N/A | ANDA | ANDA203244 | Proficient Rx LP | GABAPENTIN | 600 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-457-90) |