| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 61919-597-90 | 61919-597 | HUMAN PRESCRIPTION DRUG | TRAMADOL HYDROCHLORIDE | TRAMADOL HYDROCHLORIDE | TABLET, FILM COATED | ORAL | 20200723 | N/A | ANDA | ANDA090404 | DirectRX | TRAMADOL HYDROCHLORIDE | 50 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-597-90) |
| 61919-597-30 | 61919-597 | HUMAN PRESCRIPTION DRUG | TRAMADOL HYDROCHLORIDE | TRAMADOL HYDROCHLORIDE | TABLET, FILM COATED | ORAL | 20200723 | N/A | ANDA | ANDA090404 | DirectRX | TRAMADOL HYDROCHLORIDE | 50 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-597-30) |
| 61919-597-40 | 61919-597 | HUMAN PRESCRIPTION DRUG | TRAMADOL HYDROCHLORIDE | TRAMADOL HYDROCHLORIDE | TABLET, FILM COATED | ORAL | 20200723 | N/A | ANDA | ANDA090404 | DirectRX | TRAMADOL HYDROCHLORIDE | 50 mg/1 | 40 TABLET, FILM COATED in 1 BOTTLE (61919-597-40) |
| 61919-597-60 | 61919-597 | HUMAN PRESCRIPTION DRUG | TRAMADOL HYDROCHLORIDE | TRAMADOL HYDROCHLORIDE | TABLET, FILM COATED | ORAL | 20200723 | N/A | ANDA | ANDA090404 | DirectRX | TRAMADOL HYDROCHLORIDE | 50 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (61919-597-60) |