| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72189-073-30 | 72189-073 | HUMAN PRESCRIPTION DRUG | LEVOTHYROXINE SODIUM | LEVOTHYROXINE SODIUM | TABLET | ORAL | 20200730 | N/A | NDA | NDA021116 | DIRECT RX | LEVOTHYROXINE SODIUM | 75 ug/1 | 30 TABLET in 1 BOTTLE (72189-073-30) |
| 71205-352-30 | 71205-352 | HUMAN PRESCRIPTION DRUG | levothyroxine sodium | levothyroxine sodium | TABLET | ORAL | 20191101 | N/A | NDA | NDA021116 | Proficient Rx LP | LEVOTHYROXINE SODIUM | 50 ug/1 | 30 TABLET in 1 BOTTLE (71205-352-30) |
| 71205-352-60 | 71205-352 | HUMAN PRESCRIPTION DRUG | levothyroxine sodium | levothyroxine sodium | TABLET | ORAL | 20191101 | N/A | NDA | NDA021116 | Proficient Rx LP | LEVOTHYROXINE SODIUM | 50 ug/1 | 60 TABLET in 1 BOTTLE (71205-352-60) |
| 71205-352-90 | 71205-352 | HUMAN PRESCRIPTION DRUG | levothyroxine sodium | levothyroxine sodium | TABLET | ORAL | 20191101 | N/A | NDA | NDA021116 | Proficient Rx LP | LEVOTHYROXINE SODIUM | 50 ug/1 | 90 TABLET in 1 BOTTLE (71205-352-90) |
| 72189-073-90 | 72189-073 | HUMAN PRESCRIPTION DRUG | LEVOTHYROXINE SODIUM | LEVOTHYROXINE SODIUM | TABLET | ORAL | 20200730 | N/A | NDA | NDA021116 | DIRECT RX | LEVOTHYROXINE SODIUM | 75 ug/1 | 90 TABLET in 1 BOTTLE (72189-073-90) |