| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 67877-878-20 | 67877-878 | HUMAN PRESCRIPTION DRUG | Cefpodoxime Proxetil | Cefpodoxime Proxetil | TABLET, FILM COATED | ORAL | 20230301 | N/A | ANDA | ANDA210568 | Ascend Laboratories, LLC | CEFPODOXIME PROXETIL | 100 mg/1 | 20 TABLET, FILM COATED in 1 BOTTLE (67877-878-20) |
| 67877-879-01 | 67877-879 | HUMAN PRESCRIPTION DRUG | Cefpodoxime Proxetil | Cefpodoxime Proxetil | TABLET, FILM COATED | ORAL | 20230301 | N/A | ANDA | ANDA210568 | Ascend Laboratories, LLC | CEFPODOXIME PROXETIL | 200 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-879-01) |
| 67877-879-05 | 67877-879 | HUMAN PRESCRIPTION DRUG | Cefpodoxime Proxetil | Cefpodoxime Proxetil | TABLET, FILM COATED | ORAL | 20230301 | N/A | ANDA | ANDA210568 | Ascend Laboratories, LLC | CEFPODOXIME PROXETIL | 200 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-879-05) |
| 67877-879-20 | 67877-879 | HUMAN PRESCRIPTION DRUG | Cefpodoxime Proxetil | Cefpodoxime Proxetil | TABLET, FILM COATED | ORAL | 20230213 | N/A | ANDA | ANDA210568 | Ascend Laboratories, LLC | CEFPODOXIME PROXETIL | 200 mg/1 | 20 TABLET, FILM COATED in 1 BOTTLE (67877-879-20) |