| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63629-3816-1 | 63629-3816 | HUMAN PRESCRIPTION DRUG | OXCARBAZEPINE | OXCARBAZEPINE | TABLET, FILM COATED | ORAL | 20110728 | N/A | ANDA | ANDA078069 | Bryant Ranch Prepack | OXCARBAZEPINE | 150 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-3816-1) |
| 63629-3816-3 | 63629-3816 | HUMAN PRESCRIPTION DRUG | OXCARBAZEPINE | OXCARBAZEPINE | TABLET, FILM COATED | ORAL | 20120806 | N/A | ANDA | ANDA078069 | Bryant Ranch Prepack | OXCARBAZEPINE | 150 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-3816-3) |
| 63629-3816-2 | 63629-3816 | HUMAN PRESCRIPTION DRUG | OXCARBAZEPINE | OXCARBAZEPINE | TABLET, FILM COATED | ORAL | 20081014 | N/A | ANDA | ANDA078069 | Bryant Ranch Prepack | OXCARBAZEPINE | 150 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-3816-2) |
| 63629-9186-1 | 63629-9186 | HUMAN PRESCRIPTION DRUG | OXCARBAZEPINE | OXCARBAZEPINE | TABLET, FILM COATED | ORAL | 20220803 | N/A | ANDA | ANDA078069 | Bryant Ranch Prepack | OXCARBAZEPINE | 300 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (63629-9186-1) |