美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SPIRONOLACTONE W/ 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
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 085974 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 086026 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 087004 002 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- 1982/05/24 IVAX PHARMS Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 087511 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- Approved Prior to Jan 1, 1982 LEDERLE Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 087553 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- Approved Prior to Jan 1, 1982 UPSHER SMITH Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 087651 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- Approved Prior to Jan 1, 1982 USL PHARMA Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 087948 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- 1983/02/22 PARKE DAVIS Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 088054 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- 1983/08/18 PUREPAC PHARM Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 087655 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1981/12/14 Approved Prior to Jan 1, 1982 VANGARD Discontinued
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