美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=HYDROCHLOROTHIAZIDE"
符合检索条件的记录共 788 条
共 40 页，当前第 5 页
首页 上一页 下一页 最后一页 返回检索页 可点击列名称排序
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
HYDROCHLOROTHIAZIDE W/ RESERPINE 083568 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 50MG;0.1MG No No 1973/12/04 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE 083573 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 50MG;0.125MG No No 1973/12/11 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
HYDROCHLOROTHIAZIDE 083809 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1974/07/02 Approved Prior to Jan 1, 1982 WHITEWORTH TOWN PLSN Discontinued
HYDROCHLOROTHIAZIDE 083809 002 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1974/07/02 Approved Prior to Jan 1, 1982 WHITEWORTH TOWN PLSN Discontinued
HYDROCHLOROTHIAZIDE 083972 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1974/10/03 Approved Prior to Jan 1, 1982 SUN PHARM INDUSTRIES Discontinued
HYDROCHLOROTHIAZIDE 083972 002 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1974/10/03 Approved Prior to Jan 1, 1982 SUN PHARM INDUSTRIES Discontinued
HYDROCHLOROTHIAZIDE 083972 003 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 100MG No No 1974/10/03 Approved Prior to Jan 1, 1982 SUN PHARM INDUSTRIES Discontinued
HYDROCHLOROTHIAZIDE 083232 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1975/01/24 Approved Prior to Jan 1, 1982 WATSON LABS TEVA Discontinued
HYDRALAZINE HYDROCHLORIDE, HYDROCHLOROTHIAZIDE AND RESERPINE 084291 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 25MG;15MG;0.1MG No No 1975/02/03 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
RESERPINE AND HYDROCHLOROTHIAZIDE 084580 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 25MG;0.125MG No No 1975/05/30 Approved Prior to Jan 1, 1982 BARR Discontinued
HYDROCHLOROTHIAZIDE 084658 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1975/09/24 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
RESERPINE AND HYDROCHLOROTHIAZIDE 084579 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 50MG;0.125MG No No 1975/09/30 Approved Prior to Jan 1, 1982 BARR Discontinued
HYDROCHLOROTHIAZIDE 084324 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1976/06/24 Approved Prior to Jan 1, 1982 LANNETT CO INC Discontinued
HYDROCHLOROTHIAZIDE 084325 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1976/06/24 Approved Prior to Jan 1, 1982 LANNETT CO INC Discontinued
HYDROCHLOROTHIAZIDE 084776 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1976/09/21 Approved Prior to Jan 1, 1982 INWOOD LABS Discontinued
HYDROCHLOROTHIAZIDE 084776 002 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1976/09/21 Approved Prior to Jan 1, 1982 INWOOD LABS Discontinued
HYDROCHLOROTHIAZIDE 084912 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1976/12/17 Approved Prior to Jan 1, 1982 CHARTWELL RX Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE 084466 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 25MG;0.125MG No No 1977/01/07 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE 084467 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 50MG;0.125MG No No 1977/01/07 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 084878 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1977/01/31 Approved Prior to Jan 1, 1982 HIKMA INTL PHARMS Discontinued
药品名称，活性成分，申请号搜索 高级检索
©2006-2024 DrugFuture->U.S. FDA Drugs Database