| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1987-2 | 71335-1987 | HUMAN PRESCRIPTION DRUG | Levothyroxine Sodium | Levothyroxine Sodium | TABLET | ORAL | 20240531 | N/A | NDA AUTHORIZED GENERIC | NDA021342 | Bryant Ranch Prepack | LEVOTHYROXINE SODIUM | 137 ug/1 | 100 TABLET in 1 BOTTLE (71335-1987-2) |
| 71335-1987-3 | 71335-1987 | HUMAN PRESCRIPTION DRUG | Levothyroxine Sodium | Levothyroxine Sodium | TABLET | ORAL | 20211110 | N/A | NDA AUTHORIZED GENERIC | NDA021342 | Bryant Ranch Prepack | LEVOTHYROXINE SODIUM | 137 ug/1 | 90 TABLET in 1 BOTTLE (71335-1987-3) |
| 71335-1987-4 | 71335-1987 | HUMAN PRESCRIPTION DRUG | Levothyroxine Sodium | Levothyroxine Sodium | TABLET | ORAL | 20240531 | N/A | NDA AUTHORIZED GENERIC | NDA021342 | Bryant Ranch Prepack | LEVOTHYROXINE SODIUM | 137 ug/1 | 28 TABLET in 1 BOTTLE (71335-1987-4) |
| 71335-1987-5 | 71335-1987 | HUMAN PRESCRIPTION DRUG | Levothyroxine Sodium | Levothyroxine Sodium | TABLET | ORAL | 20240531 | N/A | NDA AUTHORIZED GENERIC | NDA021342 | Bryant Ranch Prepack | LEVOTHYROXINE SODIUM | 137 ug/1 | 60 TABLET in 1 BOTTLE (71335-1987-5) |
| 72162-1092-0 | 72162-1092 | HUMAN PRESCRIPTION DRUG | Levothyroxine Sodium | Levothyroxine Sodium | TABLET | ORAL | 20200803 | N/A | NDA AUTHORIZED GENERIC | NDA021342 | Bryant Ranch Prepack | LEVOTHYROXINE SODIUM | 137 ug/1 | 1000 TABLET in 1 BOTTLE (72162-1092-0) |