| 商品名 | 申请号 | 产品号 | 申请类型 | 活性成分 | 剂型/给药途径 | 规格/剂量 | RLD | RS | 申请号原始批准/暂定批准日期 | 产品号批准日期 | 申请人 | 市场状态 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| WELLCOVORIN | 018342 | 001 | NDA | LEUCOVORIN CALCIUM | TABLET;ORAL | EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | -- | 1983/07/08 | GLAXOSMITHKLINE | Discontinued |
| WELLCOVORIN | 018342 | 002 | NDA | LEUCOVORIN CALCIUM | TABLET;ORAL | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | -- | 1983/07/08 | GLAXOSMITHKLINE | Discontinued |
| WELLCOVORIN | 087439 | 001 | ANDA | LEUCOVORIN CALCIUM | INJECTABLE;INJECTION | EQ 5MG BASE/ML | No | No | -- | 1982/10/19 | GLAXOSMITHKLINE | Discontinued |
| WELLCOVORIN | 089465 | 001 | ANDA | LEUCOVORIN CALCIUM | INJECTABLE;INJECTION | EQ 50MG BASE/VIAL | No | No | -- | 1989/01/23 | GLAXOSMITHKLINE | Discontinued |
| WELLCOVORIN | 089833 | 001 | ANDA | LEUCOVORIN CALCIUM | INJECTABLE;INJECTION | EQ 25MG BASE/VIAL | No | No | -- | 1989/01/23 | GLAXOSMITHKLINE | Discontinued |
| WELLCOVORIN | 089834 | 001 | ANDA | LEUCOVORIN CALCIUM | INJECTABLE;INJECTION | EQ 100MG BASE/VIAL | No | No | -- | 1989/01/23 | GLAXOSMITHKLINE | Discontinued |