| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 80425-0422-2 | 80425-0422 | HUMAN PRESCRIPTION DRUG | Ibuprofen and famotidine | Ibuprofen and famotidine | TABLET, FILM COATED | ORAL | 20240716 | N/A | ANDA | ANDA211890 | Advanced Rx of Tennessee, LLC | FAMOTIDINE; IBUPROFEN | 26.6 mg/1; 800 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (80425-0422-2) |
| 80425-0422-3 | 80425-0422 | HUMAN PRESCRIPTION DRUG | Ibuprofen and famotidine | Ibuprofen and famotidine | TABLET, FILM COATED | ORAL | 20240716 | N/A | ANDA | ANDA211890 | Advanced Rx of Tennessee, LLC | FAMOTIDINE; IBUPROFEN | 26.6 mg/1; 800 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (80425-0422-3) |