美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE"
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
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 077483 001 ANDA BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL 5MG;6.25MG No No 2005/09/08 2005/09/08 SUN PHARM INDS LTD Discontinued
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 077483 002 ANDA BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL 10MG;12.5MG No No 2005/09/08 2005/09/08 SUN PHARM INDS LTD Discontinued
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 077483 003 ANDA BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL 20MG;12.5MG No No 2005/09/08 2005/09/08 SUN PHARM INDS LTD Discontinued
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 077483 004 ANDA BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL 20MG;25MG No No 2005/09/08 2005/09/08 SUN PHARM INDS LTD Discontinued
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 078794 001 ANDA BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL 5MG;6.25MG No No 2014/08/21 2014/08/21 APOTEX Prescription
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 078794 002 ANDA BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL 10MG;12.5MG No No 2014/08/21 2014/08/21 APOTEX Prescription
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 078794 003 ANDA BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL 20MG;12.5MG No No 2014/08/21 2014/08/21 APOTEX Prescription
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 078794 004 ANDA BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL 20MG;25MG No No 2014/08/21 2014/08/21 APOTEX Prescription
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