| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 42847-850-09 | 42847-850 | HUMAN PRESCRIPTION DRUG | Treximet | Sumatriptan Succinate and Naproxen Sodium | TABLET, FILM COATED | ORAL | 20080425 | N/A | NDA | NDA021926 | Currax Pharmaceuticals LLC | NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE | 500 mg/1; 85 mg/1 | 9 TABLET, FILM COATED in 1 BOTTLE (42847-850-09) |
| 44183-850-09 | 44183-850 | HUMAN PRESCRIPTION DRUG | Sumatriptan Succinate and Naproxen Sodium | sumatriptan succinate and naproxen sodium | TABLET | ORAL | 20180215 | N/A | NDA AUTHORIZED GENERIC | NDA021926 | Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven | NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE | 500 mg/1; 85 mg/1 | 9 TABLET in 1 BOTTLE (44183-850-09) |