| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-2048-1 | 71335-2048 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20220315 | N/A | ANDA | ANDA206402 | Bryant Ranch Prepack | GABAPENTIN | 600 mg/1 | 90 TABLET in 1 BOTTLE (71335-2048-1) |
| 71335-2048-2 | 71335-2048 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20250130 | N/A | ANDA | ANDA206402 | Bryant Ranch Prepack | GABAPENTIN | 600 mg/1 | 58 TABLET in 1 BOTTLE (71335-2048-2) |
| 71335-2048-3 | 71335-2048 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20221227 | N/A | ANDA | ANDA206402 | Bryant Ranch Prepack | GABAPENTIN | 600 mg/1 | 100 TABLET in 1 BOTTLE (71335-2048-3) |
| 71335-2048-4 | 71335-2048 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20220322 | N/A | ANDA | ANDA206402 | Bryant Ranch Prepack | GABAPENTIN | 600 mg/1 | 120 TABLET in 1 BOTTLE (71335-2048-4) |
| 71335-2048-5 | 71335-2048 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20220221 | N/A | ANDA | ANDA206402 | Bryant Ranch Prepack | GABAPENTIN | 600 mg/1 | 60 TABLET in 1 BOTTLE (71335-2048-5) |
| 71335-2048-6 | 71335-2048 | HUMAN PRESCRIPTION DRUG | Gabapentin | Gabapentin | TABLET | ORAL | 20230621 | N/A | ANDA | ANDA206402 | Bryant Ranch Prepack | GABAPENTIN | 600 mg/1 | 30 TABLET in 1 BOTTLE (71335-2048-6) |