| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70518-2370-0 | 70518-2370 | HUMAN PRESCRIPTION DRUG | OXCARBAZEPINE | OXCARBAZEPINE | TABLET, FILM COATED | ORAL | 20191019 | N/A | ANDA | ANDA078069 | REMEDYREPACK INC. | OXCARBAZEPINE | 300 mg/1 | 100 POUCH in 1 BOX (70518-2370-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-2370-1) |
| 70518-2370-2 | 70518-2370 | HUMAN PRESCRIPTION DRUG | OXCARBAZEPINE | OXCARBAZEPINE | TABLET, FILM COATED | ORAL | 20241004 | N/A | ANDA | ANDA078069 | REMEDYREPACK INC. | OXCARBAZEPINE | 300 mg/1 | 100 POUCH in 1 BOX (70518-2370-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-2370-3) |