| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 13107-079-30 | 13107-079 | HUMAN PRESCRIPTION DRUG | TRAZODONE HYDROCHLORIDE | TRAZODONE HYDROCHLORIDE | TABLET | ORAL | 20150915 | N/A | ANDA | ANDA204852 | Aurolife Pharma LLC | TRAZODONE HYDROCHLORIDE | 50 mg/1 | 30 TABLET in 1 BOTTLE (13107-079-30) |
| 13107-079-01 | 13107-079 | HUMAN PRESCRIPTION DRUG | TRAZODONE HYDROCHLORIDE | TRAZODONE HYDROCHLORIDE | TABLET | ORAL | 20150915 | N/A | ANDA | ANDA204852 | Aurolife Pharma LLC | TRAZODONE HYDROCHLORIDE | 50 mg/1 | 100 TABLET in 1 BOTTLE (13107-079-01) |
| 13107-080-30 | 13107-080 | HUMAN PRESCRIPTION DRUG | TRAZODONE HYDROCHLORIDE | TRAZODONE HYDROCHLORIDE | TABLET | ORAL | 20150915 | N/A | ANDA | ANDA204852 | Aurolife Pharma LLC | TRAZODONE HYDROCHLORIDE | 100 mg/1 | 30 TABLET in 1 BOTTLE (13107-080-30) |