| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0093-5261-29 | 0093-5261 | HUMAN PRESCRIPTION DRUG | Almotriptan Malate | Almotriptan Malate | TABLET, FILM COATED | ORAL | 20150707 | N/A | ANDA | ANDA078027 | Teva Pharmaceuticals USA, Inc. | ALMOTRIPTAN MALATE | 12.5 mg/1 | 12 BLISTER PACK in 1 CARTON (0093-5261-29) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-5261-19) |
| 0093-5260-18 | 0093-5260 | HUMAN PRESCRIPTION DRUG | Almotriptan Malate | Almotriptan Malate | TABLET, FILM COATED | ORAL | 20150707 | N/A | ANDA | ANDA078027 | Teva Pharmaceuticals USA, Inc. | ALMOTRIPTAN MALATE | 6.25 mg/1 | 6 BLISTER PACK in 1 CARTON (0093-5260-18) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-5260-19) |