美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ZIDE"
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
TRICHLORMETHIAZIDE 083847 001 ANDA TRICHLORMETHIAZIDE TABLET;ORAL 2MG No No 1978/02/06 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
CHLOROTHIAZIDE 085569 001 ANDA CHLOROTHIAZIDE TABLET;ORAL 250MG No No 1978/03/08 Approved Prior to Jan 1, 1982 ABC HOLDING Discontinued
HYDRALAZINE, HYDROCHLOROTHIAZIDE W/ RESERPINE 085771 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 25MG;15MG;0.1MG No No 1978/04/21 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE 086330 002 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 25MG;0.125MG No No 1978/06/12 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE 086331 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 50MG;0.125MG No No 1978/06/12 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 085004 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1978/07/13 Approved Prior to Jan 1, 1982 ROXANE Discontinued
HYDROCHLOROTHIAZIDE 085005 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1978/07/13 Approved Prior to Jan 1, 1982 ROXANE Discontinued
HYDROCHLOROTHIAZIDE 086087 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1978/07/17 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 086594 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1978/10/05 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 086597 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1978/10/11 Approved Prior to Jan 1, 1982 PVT FORM Discontinued
TRICHLORMETHIAZIDE 086458 001 ANDA TRICHLORMETHIAZIDE TABLET;ORAL 2MG No No 1978/10/31 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 085219 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 1979/03/12 Approved Prior to Jan 1, 1982 AUROLIFE PHARMA LLC 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 W/ HYDROCHLOROTHIAZIDE 087004 002 ANDA HYDROCHLOROTHIAZIDE; SPIRONOLACTONE TABLET;ORAL 25MG;25MG No No 1980/05/07 1982/05/24 IVAX PHARMS Discontinued
MINIZIDE 017986 001 NDA POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE CAPSULE;ORAL 0.5MG;EQ 1MG BASE No No 1980/06/13 Approved Prior to Jan 1, 1982 PFIZER Discontinued
MINIZIDE 017986 002 NDA POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE CAPSULE;ORAL 0.5MG;EQ 2MG BASE No No 1980/06/13 Approved Prior to Jan 1, 1982 PFIZER Discontinued
MINIZIDE 017986 003 NDA POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE CAPSULE;ORAL 0.5MG;EQ 5MG BASE No No 1980/06/13 Approved Prior to Jan 1, 1982 PFIZER 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
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