| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1007-8 | 71335-1007 | HUMAN PRESCRIPTION DRUG | Gabapentin | GABAPENTIN | TABLET, FILM COATED | ORAL | 20240409 | N/A | ANDA | ANDA203244 | Bryant Ranch Prepack | GABAPENTIN | 800 mg/1 | 112 TABLET, FILM COATED in 1 BOTTLE (71335-1007-8) |
| 71335-1007-9 | 71335-1007 | HUMAN PRESCRIPTION DRUG | Gabapentin | GABAPENTIN | TABLET, FILM COATED | ORAL | 20240409 | N/A | ANDA | ANDA203244 | Bryant Ranch Prepack | GABAPENTIN | 800 mg/1 | 135 TABLET, FILM COATED in 1 BOTTLE (71335-1007-9) |
| 72162-2141-5 | 72162-2141 | HUMAN PRESCRIPTION DRUG | Gabapentin | GABAPENTIN | TABLET, FILM COATED | ORAL | 20231012 | N/A | ANDA | ANDA203244 | Bryant Ranch Prepack | GABAPENTIN | 600 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-2141-5) |