| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 68308-475-47 | 68308-475 | HUMAN PRESCRIPTION DRUG | Oxycodone and Acetaminophen | Oxycodone Hydrochloride and Acetaminophen | TABLET | ORAL | 20081216 | N/A | ANDA | ANDA090177 | Mayne Pharma Inc. | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 325 mg/1; 7.5 mg/1 | 10 BLISTER PACK in 1 CARTON (68308-475-47) / 10 TABLET in 1 BLISTER PACK |
| 68308-480-47 | 68308-480 | HUMAN PRESCRIPTION DRUG | Oxycodone and Acetaminophen | Oxycodone Hydrochloride and Acetaminophen | TABLET | ORAL | 20081216 | N/A | ANDA | ANDA090177 | Mayne Pharma Inc. | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 325 mg/1; 10 mg/1 | 10 BLISTER PACK in 1 CARTON (68308-480-47) / 10 TABLET in 1 BLISTER PACK |