| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0173-0736-01 | 0173-0736 | HUMAN PRESCRIPTION DRUG | IMITREX | sumatriptan | TABLET, FILM COATED | ORAL | 20031217 | N/A | NDA | NDA020132 | GlaxoSmithKline LLC | SUMATRIPTAN SUCCINATE | 50 mg/1 | 1 CARTON in 1 CARTON (0173-0736-01) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK |
| 0173-0737-01 | 0173-0737 | HUMAN PRESCRIPTION DRUG | IMITREX | sumatriptan | TABLET, FILM COATED | ORAL | 20031219 | N/A | NDA | NDA020132 | GlaxoSmithKline LLC | SUMATRIPTAN SUCCINATE | 100 mg/1 | 1 CARTON in 1 CARTON (0173-0737-01) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK |
| 0173-0735-00 | 0173-0735 | HUMAN PRESCRIPTION DRUG | IMITREX | sumatriptan | TABLET, FILM COATED | ORAL | 20031217 | N/A | NDA | NDA020132 | GlaxoSmithKline LLC | SUMATRIPTAN SUCCINATE | 25 mg/1 | 1 CARTON in 1 CARTON (0173-0735-00) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK |