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
VISKAZIDE 018872 001 NDA HYDROCHLOROTHIAZIDE; PINDOLOL TABLET;ORAL 25MG;5MG No No -- 1987/07/22 NOVARTIS Discontinued
VISKAZIDE 018872 002 NDA HYDROCHLOROTHIAZIDE; PINDOLOL TABLET;ORAL 25MG;10MG No No -- 1987/07/22 NOVARTIS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070365 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No -- 1986/03/19 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070366 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No -- 1986/04/16 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070367 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No -- 1986/03/19 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070368 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No -- 1986/04/16 WATSON LABS Discontinued
METHYLDOPA AND CHLOROTHIAZIDE 070654 001 ANDA CHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 250MG;250MG No No -- 1987/11/06 PAR PHARM Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070688 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No -- 1986/04/24 PUREPAC PHARM Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070689 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No -- 1986/04/24 PUREPAC PHARM Discontinued
METHYLDOPA AND CHLOROTHIAZIDE 070783 001 ANDA CHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 150MG;250MG No No -- 1987/11/06 PAR PHARM Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070829 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No -- 1987/03/09 SANDOZ Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070830 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No -- 1987/03/09 SANDOZ Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070853 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No -- 1986/10/08 PUREPAC PHARM Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070854 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No -- 1986/10/08 PUREPAC PHARM Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071458 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No -- 1988/03/08 IVAX SUB TEVA PHARMS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071459 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No -- 1988/03/08 IVAX SUB TEVA PHARMS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071460 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No -- 1988/03/08 IVAX SUB TEVA PHARMS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 071461 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No -- 1988/03/08 IVAX SUB TEVA PHARMS Discontinued
PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 071552 001 ANDA HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE TABLET;ORAL 25MG;40MG No No -- 1988/12/01 IVAX SUB TEVA PHARMS Discontinued
PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 071553 001 ANDA HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE TABLET;ORAL 25MG;80MG No No -- 1988/12/01 IVAX SUB TEVA PHARMS Discontinued
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