| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 52605-022-10 | 52605-022 | HUMAN PRESCRIPTION DRUG | Phentermine hydrochloride | Phentermine hydrochloride | TABLET | ORAL | 20161118 | N/A | ANDA | ANDA206342 | POLYGEN PHARMACEUTICALS INC. | PHENTERMINE HYDROCHLORIDE | 37.5 mg/1 | 1000 TABLET in 1 BOTTLE (52605-022-10) |
| 52605-022-01 | 52605-022 | HUMAN PRESCRIPTION DRUG | Phentermine hydrochloride | Phentermine hydrochloride | TABLET | ORAL | 20161118 | N/A | ANDA | ANDA206342 | POLYGEN PHARMACEUTICALS INC. | PHENTERMINE HYDROCHLORIDE | 37.5 mg/1 | 100 TABLET in 1 BOTTLE (52605-022-01) |