美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=METHYLDOPA AND HYDROCHLOROTHIAZIDE"
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 071922 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No -- 1988/08/29 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071923 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No -- 1988/08/29 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070182 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No 1986/01/15 1986/01/15 CHARTWELL RX Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070183 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No 1986/01/15 1986/01/15 CHARTWELL RX Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070543 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No 1986/01/15 1986/01/15 CHARTWELL RX Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070544 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No 1986/01/15 1986/01/15 CHARTWELL RX Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070265 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No 1986/01/23 1986/01/23 RISING Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070265 002 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No 1986/01/23 1986/01/23 RISING Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070612 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No 1987/02/02 1987/02/02 STRIDES PHARMA Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070613 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No 1987/02/02 1987/02/02 STRIDES PHARMA Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070614 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No 1987/02/02 1987/02/02 STRIDES PHARMA Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070616 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No 1987/02/02 1987/02/02 STRIDES PHARMA Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071819 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No 1988/04/08 1988/04/08 TEVA Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071820 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No 1988/04/08 1988/04/08 TEVA Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071821 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No 1988/04/08 1988/04/08 TEVA Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071822 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No 1988/04/08 1988/04/08 TEVA Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070959 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No 1989/01/19 1989/01/19 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071069 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No 1989/01/19 1989/01/19 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070958 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No 1989/02/06 1989/02/06 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070960 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No 1989/02/06 1989/02/06 WATSON LABS Discontinued
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