| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CELEXA | 020822 | 001 | NDA | CITALOPRAM HYDROBROMIDE | TABLET;ORAL | EQ 10MG BASE | Yes | No | 1998/07/17 | 2000/04/27 | ABBVIE | Prescription |
| CELEXA | 020822 | 002 | NDA | CITALOPRAM HYDROBROMIDE | TABLET;ORAL | EQ 20MG BASE | Yes | No | 1998/07/17 | 1998/07/17 | ABBVIE | Prescription |
| CELEXA | 020822 | 003 | NDA | CITALOPRAM HYDROBROMIDE | TABLET;ORAL | EQ 40MG BASE | Yes | Yes | 1998/07/17 | 1998/07/17 | ABBVIE | Prescription |
| CELEXA | 020822 | 004 | NDA | CITALOPRAM HYDROBROMIDE | TABLET;ORAL | EQ 60MG BASE | No | No | 1998/07/17 | 1998/07/17 | ABBVIE | Discontinued |
| CELEXA | 021046 | 001 | NDA | CITALOPRAM HYDROBROMIDE | SOLUTION;ORAL | EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | 1999/12/22 | 1999/12/22 | FOREST LABS | Discontinued |