美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CHLOROTHIAZIDE"
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 086513 001 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1979/08/03 Approved Prior to Jan 1, 1982 MYLAN Prescription
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE 087004 002 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1980/05/07 1982/05/24 IVAX PHARMS Discontinued
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
HYDROCHLOROTHIAZIDE 087059 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1980/11/05 Approved Prior to Jan 1, 1982 OXFORD PHARMS Prescription
HYDROCHLOROTHIAZIDE 087060 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 100MG No No 1980/11/05 Approved Prior to Jan 1, 1982 DAVA PHARMS INC Discontinued
HYDROCHLOROTHIAZIDE 087068 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1980/11/05 Approved Prior to Jan 1, 1982 OXFORD PHARMS Prescription
HYDROCHLOROTHIAZIDE 087002 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 100MG No No 1981/02/09 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
CHLOROTHIAZIDE 085485 001 ANDA CHLOROTHIAZIDE TABLET;ORAL 250MG No No 1981/04/01 Approved Prior to Jan 1, 1982 SANDOZ 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
RESERPINE, HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 087556 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 25MG;15MG;0.1MG No No 1981/08/06 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 085054 002 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1981/08/20 Approved Prior to Jan 1, 1982 ACTAVIS ELIZABETH Discontinued
HYDROCHLOROTHIAZIDE 085208 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1981/08/20 Approved Prior to Jan 1, 1982 ACTAVIS ELIZABETH 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
HYDROCHLOROTHIAZIDE 087610 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1981/12/07 Approved Prior to Jan 1, 1982 VANGARD 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
HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 087609 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE CAPSULE;ORAL 100MG;50MG No No 1982/02/08 1982/02/08 SOLVAY Discontinued
HYDROCHLOROTHIAZIDE 087565 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1982/03/09 1982/03/09 CHARTWELL RX Discontinued
HYDROCHLOROTHIAZIDE 087752 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1982/04/19 1982/04/19 USL PHARMA Discontinued
HYDROCHLOROTHIAZIDE 087827 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1982/04/19 1982/04/19 USL PHARMA Discontinued
CHLOROTHIAZIDE-RESERPINE 087744 001 ANDA CHLOROTHIAZIDE; RESERPINE TABLET;ORAL 250MG;0.125MG No No 1982/05/06 1982/05/06 NORVIUM BIOSCIENCE Discontinued
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