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
METHYCLOTHIAZIDE 089837 001 ANDA METHYCLOTHIAZIDE TABLET;ORAL 5MG No No 1988/08/18 1988/08/18 CHARTWELL RX Discontinued
TRIAMTERENE AND HYDROCHLOROTHIAZIDE 071851 001 ANDA HYDROCHLOROTHIAZIDE; TRIAMTERENE TABLET;ORAL 50MG;75MG No No 1988/11/30 1988/11/30 WATSON LABS Prescription
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070959 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No 1989/01/19 1989/01/19 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071069 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No 1989/01/19 1989/01/19 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070958 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No 1989/02/06 1989/02/06 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070960 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No 1989/02/06 1989/02/06 WATSON LABS Discontinued
PRINZIDE 019778 001 NDA HYDROCHLOROTHIAZIDE; LISINOPRIL TABLET;ORAL 12.5MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/02/16 1989/02/16 MERCK Discontinued
PRINZIDE 019778 002 NDA HYDROCHLOROTHIAZIDE; LISINOPRIL TABLET;ORAL 25MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/02/16 1989/02/16 MERCK Discontinued
PRINZIDE 019778 003 NDA HYDROCHLOROTHIAZIDE; LISINOPRIL TABLET;ORAL 12.5MG;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/02/16 1993/11/18 MERCK Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 072507 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No 1989/06/02 1989/06/02 DAVA PHARMS INC Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 072508 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No 1989/06/02 1989/06/02 DAVA PHARMS INC Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 072509 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No 1989/06/02 1989/06/02 DAVA PHARMS INC Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 072510 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No 1989/06/02 1989/06/02 DAVA PHARMS INC Discontinued
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 073334 001 ANDA AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL EQ 5MG ANHYDROUS;50MG No No 1991/07/19 1991/07/19 WATSON LABS Discontinued
TRIAMTERENE AND HYDROCHLOROTHIAZIDE 073191 001 ANDA HYDROCHLOROTHIAZIDE; TRIAMTERENE CAPSULE;ORAL 25MG;50MG No No 1991/07/31 1991/07/31 CHARTWELL RX Discontinued
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 073209 001 ANDA AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL EQ 5MG ANHYDROUS;50MG No Yes 1991/10/31 1991/10/31 RISING Prescription
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 073357 001 ANDA AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL EQ 5MG ANHYDROUS;50MG No No 1991/11/27 1991/11/27 CHARTWELL RX Discontinued
PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 071498 001 ANDA HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE TABLET;ORAL 25MG;40MG No No 1991/12/18 1991/12/18 WATSON LABS Discontinued
PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 071501 001 ANDA HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE TABLET;ORAL 25MG;80MG No No 1991/12/18 1991/12/18 WATSON LABS Discontinued
HYDROCHLOROTHIAZIDE 081189 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 1992/01/24 1992/01/24 WATSON LABS Discontinued
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