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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
WELLBUTRIN SR | 020358 | 001 | NDA | BUPROPION HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL | 50MG | No | No | 1996/10/04 | 1996/10/04 | GLAXOSMITHKLINE | Discontinued |
WELLBUTRIN SR | 020358 | 002 | NDA | BUPROPION HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL | 100MG | Yes | No | 1996/10/04 | 1996/10/04 | GLAXOSMITHKLINE | Prescription |
WELLBUTRIN SR | 020358 | 003 | NDA | BUPROPION HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL | 150MG | Yes | No | 1996/10/04 | 1996/10/04 | GLAXOSMITHKLINE | Prescription |
WELLBUTRIN SR | 020358 | 004 | NDA | BUPROPION HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL | 200MG | Yes | Yes | 1996/10/04 | 2002/06/14 | GLAXOSMITHKLINE | Prescription |