| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71205-016-10 | 71205-016 | HUMAN PRESCRIPTION DRUG | Metaxalone | Metaxalone | TABLET | ORAL | 20180402 | N/A | ANDA | ANDA207466 | Proficient Rx LP | METAXALONE | 800 mg/1 | 10 TABLET in 1 BOTTLE (71205-016-10) |
| 71205-016-30 | 71205-016 | HUMAN PRESCRIPTION DRUG | Metaxalone | Metaxalone | TABLET | ORAL | 20180402 | N/A | ANDA | ANDA207466 | Proficient Rx LP | METAXALONE | 800 mg/1 | 30 TABLET in 1 BOTTLE (71205-016-30) |
| 71205-016-60 | 71205-016 | HUMAN PRESCRIPTION DRUG | Metaxalone | Metaxalone | TABLET | ORAL | 20180402 | N/A | ANDA | ANDA207466 | Proficient Rx LP | METAXALONE | 800 mg/1 | 60 TABLET in 1 BOTTLE (71205-016-60) |
| 71205-016-90 | 71205-016 | HUMAN PRESCRIPTION DRUG | Metaxalone | Metaxalone | TABLET | ORAL | 20180402 | N/A | ANDA | ANDA207466 | Proficient Rx LP | METAXALONE | 800 mg/1 | 90 TABLET in 1 BOTTLE (71205-016-90) |
| 69097-998-07 | 69097-998 | HUMAN PRESCRIPTION DRUG | Metaxalone | Metaxalone | TABLET | ORAL | 20230612 | N/A | ANDA | ANDA207466 | CIPLA USA INC. | METAXALONE | 400 mg/1 | 100 TABLET in 1 BOTTLE (69097-998-07) |