| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 35356-839-30 | 35356-839 | HUMAN PRESCRIPTION DRUG | Oxycodone Hydchloride | Oxycodone Hydchloride | TABLET | ORAL | 20111220 | 20270630 | ANDA | ANDA091393 | Quality Care Products LLC | OXYCODONE HYDROCHLORIDE | 10 mg/1 | 30 TABLET in 1 BOTTLE (35356-839-30) |
| 35356-839-60 | 35356-839 | HUMAN PRESCRIPTION DRUG | Oxycodone Hydchloride | Oxycodone Hydchloride | TABLET | ORAL | 20210430 | 20270630 | ANDA | ANDA091393 | Quality Care Products LLC | OXYCODONE HYDROCHLORIDE | 10 mg/1 | 60 TABLET in 1 BOTTLE (35356-839-60) |
| 35356-839-90 | 35356-839 | HUMAN PRESCRIPTION DRUG | Oxycodone Hydchloride | Oxycodone Hydchloride | TABLET | ORAL | 20111220 | 20270630 | ANDA | ANDA091393 | Quality Care Products LLC | OXYCODONE HYDROCHLORIDE | 10 mg/1 | 90 TABLET in 1 BOTTLE (35356-839-90) |