| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-0182-3 | 71335-0182 | HUMAN PRESCRIPTION DRUG | Bupropion Hydrochloride | Bupropion Hydrochloride | TABLET, FILM COATED | ORAL | 20220928 | N/A | ANDA | ANDA076143 | Bryant Ranch Prepack | BUPROPION HYDROCHLORIDE | 100 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3) |
| 71335-0182-4 | 71335-0182 | HUMAN PRESCRIPTION DRUG | Bupropion Hydrochloride | Bupropion Hydrochloride | TABLET, FILM COATED | ORAL | 20180328 | N/A | ANDA | ANDA076143 | Bryant Ranch Prepack | BUPROPION HYDROCHLORIDE | 100 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4) |