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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
CHLOROTHIAZIDE 086028 001 ANDA CHLOROTHIAZIDE TABLET;ORAL 250MG No No 1982/07/14 1982/07/14 HIKMA INTL PHARMS Discontinued
CHLOROTHIAZIDE 087736 001 ANDA CHLOROTHIAZIDE TABLET;ORAL 500MG No No 1982/07/14 1982/07/14 HIKMA INTL PHARMS Discontinued
METHYCLOTHIAZIDE 087672 001 ANDA METHYCLOTHIAZIDE TABLET;ORAL 5MG No No 1982/08/17 1982/08/17 PHARMOBEDIENT Discontinued
CORZIDE 018647 001 NDA BENDROFLUMETHIAZIDE; NADOLOL TABLET;ORAL 5MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1983/05/25 1983/05/25 KING PHARMS LLC Discontinued
CORZIDE 018647 002 NDA BENDROFLUMETHIAZIDE; NADOLOL TABLET;ORAL 5MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1983/05/25 1983/05/25 KING PHARMS LLC Discontinued
CHLOROTHIAZIDE 086795 001 ANDA CHLOROTHIAZIDE TABLET;ORAL 250MG No No 1983/08/15 1983/08/15 WATSON LABS Discontinued
CHLOROTHIAZIDE AND RESERPINE 088365 001 ANDA CHLOROTHIAZIDE; RESERPINE TABLET;ORAL 500MG;0.125MG No No 1983/12/22 1983/12/22 HIKMA Discontinued
CHLOROTHIAZIDE AND RESERPINE 088557 001 ANDA CHLOROTHIAZIDE; RESERPINE TABLET;ORAL 250MG;0.125MG No No 1983/12/22 1983/12/22 HIKMA Discontinued
HYDRALAZINE HYDROCHLORIDE W/ HYDROCHLOROTHIAZIDE 25/25 088356 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE CAPSULE;ORAL 25MG;25MG No No 1984/04/10 1984/04/10 IVAX PHARMS Discontinued
HYDRALAZINE HYDROCHLORIDE W/ HYDROCHLOROTHIAZIDE 50/50 088357 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE CAPSULE;ORAL 50MG;50MG No No 1984/04/10 1984/04/10 IVAX PHARMS Discontinued
HYDRALAZINE HYDROCHLORIDE W/ HYDROCHLOROTHIAZIDE 100/50 088358 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE CAPSULE;ORAL 100MG;50MG No No 1984/04/10 1984/04/10 IVAX PHARMS Discontinued
RESERPINE, HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 088570 001 ANDA HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 25MG;15MG;0.1MG No No 1984/04/10 1984/04/10 SUN PHARM INDUSTRIES Discontinued
RESERPINE AND HYDROCHLOROTHIAZIDE-50 088189 001 ANDA HYDROCHLOROTHIAZIDE; RESERPINE TABLET;ORAL 50MG;0.125MG No No 1984/05/10 1984/05/10 WEST WARD Discontinued
HYDROCHLOROTHIAZIDE 088587 001 ANDA HYDROCHLOROTHIAZIDE SOLUTION;ORAL 50MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/07/02 1984/07/02 ROXANE Discontinued
HYDROCHLOROTHIAZIDE INTENSOL 088588 001 ANDA HYDROCHLOROTHIAZIDE SOLUTION;ORAL 100MG/ML No No 1984/07/02 1984/07/02 ROXANE Discontinued
METHYCLOTHIAZIDE 088724 001 ANDA METHYCLOTHIAZIDE TABLET;ORAL 5MG No No 1984/09/06 1984/09/06 WATSON LABS Discontinued
METHYCLOTHIAZIDE 088750 001 ANDA METHYCLOTHIAZIDE TABLET;ORAL 2.5MG No No 1984/09/06 1984/09/06 WATSON LABS Discontinued
CAPOZIDE 25/15 018709 001 NDA CAPTOPRIL; HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/10/12 1984/10/12 APOTHECON Discontinued
CAPOZIDE 25/25 018709 002 NDA CAPTOPRIL; HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/10/12 1984/10/12 APOTHECON Discontinued
CAPOZIDE 50/25 018709 003 NDA CAPTOPRIL; HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/10/12 1984/10/12 APOTHECON Discontinued
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