| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0049-3170-30 | 0049-3170 | HUMAN PRESCRIPTION DRUG | VFEND | voriconazole | TABLET, FILM COATED | ORAL | 20030328 | N/A | NDA | NDA021266 | Roerig | VORICONAZOLE | 50 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (0049-3170-30) |
| 0049-3180-30 | 0049-3180 | HUMAN PRESCRIPTION DRUG | VFEND | voriconazole | TABLET, FILM COATED | ORAL | 20030328 | 20270430 | NDA | NDA021266 | Roerig | VORICONAZOLE | 200 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (0049-3180-30) |
| 59762-0934-1 | 59762-0934 | HUMAN PRESCRIPTION DRUG | Voriconazole | Voriconazole | TABLET, FILM COATED | ORAL | 20171215 | N/A | NDA AUTHORIZED GENERIC | NDA021266 | Greenstone LLC | VORICONAZOLE | 50 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (59762-0934-1) |
| 59762-0936-1 | 59762-0936 | HUMAN PRESCRIPTION DRUG | Voriconazole | Voriconazole | TABLET, FILM COATED | ORAL | 20180605 | N/A | NDA AUTHORIZED GENERIC | NDA021266 | Greenstone LLC | VORICONAZOLE | 200 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (59762-0936-1) |