美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SPIRONOLACTONE 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
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 087999 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- 1985/11/06 PUREPAC PHARM Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 088025 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No -- 1984/11/23 ASCOT Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 086513 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1979/08/03 Approved Prior to Jan 1, 1982 MYLAN Prescription
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 086881 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1980/07/10 Approved Prior to Jan 1, 1982 YAOPHARMA CO LTD Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 087267 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1981/04/16 Approved Prior to Jan 1, 1982 MUTUAL PHARM Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 087398 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1981/11/24 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 089137 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1985/08/26 1985/08/26 SUPERPHARM Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 089534 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1987/07/02 1987/07/02 SUN PHARM INDUSTRIES Prescription
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