| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 67877-626-90 | 67877-626 | HUMAN PRESCRIPTION DRUG | Ibuprofen and famotidine | Ibuprofen and famotidine | TABLET, FILM COATED | ORAL | 20210804 | N/A | ANDA | ANDA211890 | Ascend Laboratories, LLC | FAMOTIDINE; IBUPROFEN | 26.6 mg/1; 800 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (67877-626-90) |
| 69306-266-30 | 69306-266 | HUMAN PRESCRIPTION DRUG | Ibuprofen and famotidine | Ibuprofen and famotidine | TABLET, FILM COATED | ORAL | 20220830 | N/A | ANDA | ANDA211890 | Doc Rx | FAMOTIDINE; IBUPROFEN | 26.6 mg/1; 800 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (69306-266-30) |