| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0173-0135-55 | 0173-0135 | HUMAN PRESCRIPTION DRUG | WELLBUTRIN SR | bupropion hydrochloride | TABLET, FILM COATED | ORAL | 19961115 | N/A | NDA | NDA020358 | GlaxoSmithKline LLC | BUPROPION HYDROCHLORIDE | 150 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (0173-0135-55) |
| 0173-0722-00 | 0173-0722 | HUMAN PRESCRIPTION DRUG | WELLBUTRIN SR | bupropion hydrochloride | TABLET, FILM COATED | ORAL | 20020625 | N/A | NDA | NDA020358 | GlaxoSmithKline LLC | BUPROPION HYDROCHLORIDE | 200 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (0173-0722-00) |
| 0173-0947-55 | 0173-0947 | HUMAN PRESCRIPTION DRUG | WELLBUTRIN SR | bupropion hydrochloride | TABLET, FILM COATED | ORAL | 19961115 | N/A | NDA | NDA020358 | GlaxoSmithKline LLC | BUPROPION HYDROCHLORIDE | 100 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (0173-0947-55) |