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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
60505-3245-3 | 60505-3245 | HUMAN PRESCRIPTION DRUG | FAMCICLOVIR | FAMCICLOVIR | TABLET, FILM COATED | ORAL | 20111220 | 20250531 | ANDA | ANDA091480 | Apotex Corp. | FAMCICLOVIR | 125 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-3245-3) |
60505-3246-3 | 60505-3246 | HUMAN PRESCRIPTION DRUG | FAMCICLOVIR | FAMCICLOVIR | TABLET, FILM COATED | ORAL | 20111220 | 20260430 | ANDA | ANDA091480 | Apotex Corp. | FAMCICLOVIR | 250 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-3246-3) |
60505-3247-3 | 60505-3247 | HUMAN PRESCRIPTION DRUG | FAMCICLOVIR | FAMCICLOVIR | TABLET, FILM COATED | ORAL | 20111220 | 20260731 | ANDA | ANDA091480 | Apotex Corp. | FAMCICLOVIR | 500 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-3247-3) |