| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70518-3940-0 | 70518-3940 | HUMAN PRESCRIPTION DRUG | Oxcarbazepine | Oxcarbazepine | TABLET, FILM COATED | ORAL | 20231206 | N/A | ANDA | ANDA215939 | REMEDYREPACK INC. | OXCARBAZEPINE | 150 mg/1 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3940-0) |
| 70518-3940-1 | 70518-3940 | HUMAN PRESCRIPTION DRUG | Oxcarbazepine | Oxcarbazepine | TABLET, FILM COATED | ORAL | 20240224 | N/A | ANDA | ANDA215939 | REMEDYREPACK INC. | OXCARBAZEPINE | 150 mg/1 | 100 POUCH in 1 BOX (70518-3940-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3940-2) |
| 82804-209-72 | 82804-209 | HUMAN PRESCRIPTION DRUG | Oxcarbazepine | Oxcarbazepine | TABLET, FILM COATED | ORAL | 20250318 | N/A | ANDA | ANDA215939 | Proficient Rx LP | OXCARBAZEPINE | 300 mg/1 | 120 TABLET, FILM COATED in 1 BOTTLE (82804-209-72) |