| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71151-031-01 | 71151-031 | HUMAN PRESCRIPTION DRUG | Mycophenolic Acid | Mycophenolic Acid | TABLET, DELAYED RELEASE | ORAL | 20240105 | N/A | ANDA | ANDA217031 | airis PHARMA Private Limited | MYCOPHENOLATE SODIUM | 360 mg/1 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71151-031-01) |
| 71151-030-01 | 71151-030 | HUMAN PRESCRIPTION DRUG | Mycophenolic Acid | Mycophenolic Acid | TABLET, DELAYED RELEASE | ORAL | 20240105 | N/A | ANDA | ANDA217031 | airis PHARMA Private Limited | MYCOPHENOLATE SODIUM | 180 mg/1 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71151-030-01) |