商品名 | 申请号 | 产品号 | 申请类型 | 活性成分 | 剂型/给药途径 | 规格/剂量 | RLD | RS | 申请号原始批准/暂定批准日期 | 产品号批准日期 | 申请人 | 市场状态 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
METHYLDOPA AND HYDROCHLOROTHIAZIDE | 072507 | 001 | ANDA | HYDROCHLOROTHIAZIDE; METHYLDOPA | TABLET;ORAL | 15MG;250MG | No | No | 1989/06/02 | 1989/06/02 | DAVA PHARMS INC | Discontinued |
METHYLDOPA AND HYDROCHLOROTHIAZIDE | 072508 | 001 | ANDA | HYDROCHLOROTHIAZIDE; METHYLDOPA | TABLET;ORAL | 25MG;250MG | No | No | 1989/06/02 | 1989/06/02 | DAVA PHARMS INC | Discontinued |
METHYLDOPA AND HYDROCHLOROTHIAZIDE | 072509 | 001 | ANDA | HYDROCHLOROTHIAZIDE; METHYLDOPA | TABLET;ORAL | 30MG;500MG | No | No | 1989/06/02 | 1989/06/02 | DAVA PHARMS INC | Discontinued |
METHYLDOPA AND HYDROCHLOROTHIAZIDE | 072510 | 001 | ANDA | HYDROCHLOROTHIAZIDE; METHYLDOPA | TABLET;ORAL | 50MG;500MG | No | No | 1989/06/02 | 1989/06/02 | DAVA PHARMS INC | Discontinued |