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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
59651-621-08 | 59651-621 | HUMAN PRESCRIPTION DRUG | MYCOPHENOLIC ACID | MYCOPHENOLIC ACID | TABLET, DELAYED RELEASE | ORAL | 20240227 | N/A | ANDA | ANDA218603 | Aurobindo Pharma Limited | MYCOPHENOLATE SODIUM | 180 mg/1 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-621-08) |
59651-622-08 | 59651-622 | HUMAN PRESCRIPTION DRUG | MYCOPHENOLIC ACID | MYCOPHENOLIC ACID | TABLET, DELAYED RELEASE | ORAL | 20240227 | N/A | ANDA | ANDA218603 | Aurobindo Pharma Limited | MYCOPHENOLATE SODIUM | 360 mg/1 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-622-08) |