| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 59762-5030-1 | 59762-5030 | HUMAN PRESCRIPTION DRUG | Fluconazole | fluconazole | POWDER, FOR SUSPENSION | ORAL | 19931223 | N/A | NDA AUTHORIZED GENERIC | NDA020090 | Greenstone LLC | FLUCONAZOLE | 40 mg/mL | 1 BOTTLE in 1 CARTON (59762-5030-1) / 35 mL in 1 BOTTLE |
| 0049-3440-19 | 0049-3440 | HUMAN PRESCRIPTION DRUG | Diflucan | fluconazole | POWDER, FOR SUSPENSION | ORAL | 19931223 | N/A | NDA | NDA020090 | Roerig | FLUCONAZOLE | 350 mg/35mL | 1 BOTTLE in 1 CARTON (0049-3440-19) / 35 mL in 1 BOTTLE |
| 0049-3450-19 | 0049-3450 | HUMAN PRESCRIPTION DRUG | Diflucan | fluconazole | POWDER, FOR SUSPENSION | ORAL | 19931223 | N/A | NDA | NDA020090 | Roerig | FLUCONAZOLE | 1400 mg/35mL | 1 BOTTLE in 1 CARTON (0049-3450-19) / 35 mL in 1 BOTTLE |
| 59762-5029-1 | 59762-5029 | HUMAN PRESCRIPTION DRUG | Fluconazole | fluconazole | POWDER, FOR SUSPENSION | ORAL | 19931223 | N/A | NDA AUTHORIZED GENERIC | NDA020090 | Greenstone LLC | FLUCONAZOLE | 10 mg/mL | 1 BOTTLE in 1 CARTON (59762-5029-1) / 35 mL in 1 BOTTLE |