美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SPIRONOLACTONE"
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 086881 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1980/07/10 Approved Prior to Jan 1, 1982 CHARTWELL RX Discontinued
SPIRONOLACTONE 087265 001 ANDA SPIRONOLACTONE TABLET;ORAL 25MG No No 1981/01/28 Approved Prior to Jan 1, 1982 MUTUAL PHARM Discontinued
SPIRONOLACTONE 087086 001 ANDA SPIRONOLACTONE TABLET;ORAL 25MG No No 1981/02/03 Approved Prior to Jan 1, 1982 MYLAN Discontinued
SPIRONOLACTONE 087078 001 ANDA SPIRONOLACTONE TABLET;ORAL 25MG No No 1981/02/23 Approved Prior to Jan 1, 1982 WATSON LABS 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 W/ HYDROCHLOROTHIAZIDE 087655 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1981/12/14 Approved Prior to Jan 1, 1982 VANGARD Discontinued
SPIRONOLACTONE 087648 001 ANDA SPIRONOLACTONE TABLET;ORAL 25MG No No 1982/02/01 1982/02/01 VANGARD 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 087999 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1985/11/06 1985/11/06 PUREPAC PHARM Discontinued
SPIRONOLACTONE 089424 001 ANDA SPIRONOLACTONE TABLET;ORAL 25MG No No 1986/07/23 1986/07/23 SUN PHARM INDUSTRIES Prescription
SPIRONOLACTONE 089424 002 ANDA SPIRONOLACTONE TABLET;ORAL 50MG No No 1986/07/23 1999/08/11 SUN PHARM INDUSTRIES Prescription
SPIRONOLACTONE 089424 003 ANDA SPIRONOLACTONE TABLET;ORAL 100MG No No 1986/07/23 1999/08/11 SUN PHARM INDUSTRIES Prescription
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE 089534 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1987/07/02 1987/07/02 SUN PHARM INDUSTRIES Prescription
SPIRONOLACTONE 040353 001 ANDA SPIRONOLACTONE TABLET;ORAL 50MG No No 1999/07/29 1999/07/29 ACTAVIS ELIZABETH Discontinued
SPIRONOLACTONE 040353 002 ANDA SPIRONOLACTONE TABLET;ORAL 100MG No No 1999/07/29 1999/07/29 ACTAVIS ELIZABETH Discontinued
SPIRONOLACTONE 040353 003 ANDA SPIRONOLACTONE TABLET;ORAL 25MG No No 1999/07/29 2006/03/15 ACTAVIS ELIZABETH Discontinued
SPIRONOLACTONE 040424 001 ANDA SPIRONOLACTONE TABLET;ORAL 25MG No No 2001/08/20 2001/08/20 MYLAN Prescription
SPIRONOLACTONE 040424 002 ANDA SPIRONOLACTONE TABLET;ORAL 50MG No No 2001/08/20 2001/08/20 MYLAN Prescription
SPIRONOLACTONE 040424 003 ANDA SPIRONOLACTONE TABLET;ORAL 100MG No No 2001/08/20 2001/08/20 MYLAN Prescription
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