| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70512-853-60 | 70512-853 | HUMAN PRESCRIPTION DRUG | Dimethyl Fumarate | Dimethyl Fumarate | CAPSULE, DELAYED RELEASE | ORAL | 20230312 | N/A | ANDA | ANDA210436 | SOLA Pharmaceuticals, LLC | DIMETHYL FUMARATE | 240 mg/1 | 1 BOTTLE in 1 CARTON (70512-853-60) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
| 70512-852-14 | 70512-852 | HUMAN PRESCRIPTION DRUG | Dimethyl Fumarate | Dimethyl Fumarate | CAPSULE, DELAYED RELEASE | ORAL | 20230312 | N/A | ANDA | ANDA210436 | SOLA Pharmaceuticals, LLC | DIMETHYL FUMARATE | 120 mg/1 | 1 BOTTLE in 1 CARTON (70512-852-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE |