| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 59651-083-14 | 59651-083 | HUMAN PRESCRIPTION DRUG | Dimethyl Fumarate | Dimethyl Fumarate | CAPSULE, DELAYED RELEASE | ORAL | 20221222 | N/A | ANDA | ANDA210385 | Aurobindo Pharma Limited | DIMETHYL FUMARATE | 120 mg/1 | 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-083-14) |
| 59651-084-60 | 59651-084 | HUMAN PRESCRIPTION DRUG | Dimethyl Fumarate | Dimethyl Fumarate | CAPSULE, DELAYED RELEASE | ORAL | 20221222 | N/A | ANDA | ANDA210385 | Aurobindo Pharma Limited | DIMETHYL FUMARATE | 240 mg/1 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-084-60) |