| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69784-243-30 | 69784-243 | HUMAN PRESCRIPTION DRUG | Aciphex | rabeprazole sodium | TABLET, DELAYED RELEASE | ORAL | 20220515 | N/A | NDA | NDA020973 | Woodward Pharma Services LLC | RABEPRAZOLE SODIUM | 20 mg/1 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69784-243-30) |
| 80725-243-30 | 80725-243 | HUMAN PRESCRIPTION DRUG | Aciphex | rabeprazole sodium | TABLET, DELAYED RELEASE | ORAL | 20231201 | N/A | NDA | NDA020973 | Waylis Therapeutics LLC | RABEPRAZOLE SODIUM | 20 mg/1 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (80725-243-30) |