美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=CHLOROTHIAZIDE"
符合检索条件的记录共 815 条
共 41 页，当前第 2 页
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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 071897 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No -- 1987/11/23 PARKE DAVIS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071898 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No -- 1987/11/23 PARKE DAVIS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071899 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No -- 1987/11/23 PARKE DAVIS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071900 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No -- 1987/11/23 PARKE DAVIS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071920 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No -- 1988/08/29 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071921 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No -- 1988/08/29 WATSON LABS Discontinued
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
TRIAMTERENE AND HYDROCHLOROTHIAZIDE 071980 001 ANDA HYDROCHLOROTHIAZIDE; TRIAMTERENE TABLET;ORAL 50MG;75MG No No -- 1988/04/17 QUANTUM PHARMICS Discontinued
TRIAMTERENE AND HYDROCHLOROTHIAZIDE 072022 001 ANDA HYDROCHLOROTHIAZIDE; TRIAMTERENE TABLET;ORAL 50MG;75MG No No -- 1988/04/17 AM THERAP Discontinued
TRIAMTERENE AND HYDROCHLOROTHIAZIDE 074857 001 ANDA HYDROCHLOROTHIAZIDE; TRIAMTERENE CAPSULE;ORAL 25MG;37.5MG No No -- 1997/09/09 NOVARTIS Discontinued
HYDROCHLOROTHIAZIDE 083456 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 083458 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 083554 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No -- Approved Prior to Jan 1, 1982 ALRA Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE 083666 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 50MG;0.125MG No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE AND HYDRALAZINE 083770 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 25MG;15MG;0.1MG No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 083899 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 AUROLIFE PHARMA LLC Discontinued
CHLOROTHIAZIDE 084026 001 ANDA CHLOROTHIAZIDE TABLET;ORAL 500MG No No -- 1982/09/01 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 084029 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 IMPAX LABS Discontinued
HYDROCHLOROTHIAZIDE 084135 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No -- Approved Prior to Jan 1, 1982 HEATHER Discontinued
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