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
BALSALAZIDE DISODIUM 077807 001 ANDA BALSALAZIDE DISODIUM CAPSULE;ORAL 750MG No No 2007/12/28 2007/12/28 NOVITIUM PHARMA Prescription
BALSALAZIDE DISODIUM 077883 001 ANDA BALSALAZIDE DISODIUM CAPSULE;ORAL 750MG No No 2007/12/28 2007/12/28 APOTEX Prescription
GLIPIZIDE AND METFORMIN HYDROCHLORIDE 077620 001 ANDA GLIPIZIDE; METFORMIN HYDROCHLORIDE TABLET;ORAL 2.5MG;250MG No No 2008/01/11 2008/01/11 SUN PHARM INDS INC Discontinued
GLIPIZIDE AND METFORMIN HYDROCHLORIDE 077620 002 ANDA GLIPIZIDE; METFORMIN HYDROCHLORIDE TABLET;ORAL 2.5MG;500MG No No 2008/01/11 2008/01/11 SUN PHARM INDS INC Discontinued
GLIPIZIDE AND METFORMIN HYDROCHLORIDE 077620 003 ANDA GLIPIZIDE; METFORMIN HYDROCHLORIDE TABLET;ORAL 5MG;500MG No No 2008/01/11 2008/01/11 SUN PHARM INDS INC Discontinued
HYDROCHLOROTHIAZIDE 078391 001 ANDA HYDROCHLOROTHIAZIDE CAPSULE;ORAL 12.5MG No No 2008/02/11 2008/02/11 JUBILANT CADISTA Prescription
NADOLOL AND BENDROFLUMETHIAZIDE 078688 001 ANDA BENDROFLUMETHIAZIDE; NADOLOL TABLET;ORAL 5MG;40MG No No 2008/02/15 2008/02/15 NATCO PHARMA Discontinued
NADOLOL AND BENDROFLUMETHIAZIDE 078688 002 ANDA BENDROFLUMETHIAZIDE; NADOLOL TABLET;ORAL 5MG;80MG No No 2008/02/15 2008/02/15 NATCO PHARMA Discontinued
HYDROCHLOROTHIAZIDE 078389 001 ANDA HYDROCHLOROTHIAZIDE CAPSULE;ORAL 12.5MG No No 2008/05/16 2008/05/16 APOTEX Discontinued
HYDROCHLOROTHIAZIDE 040857 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 12.5MG No No 2008/05/30 2008/05/30 SUN PHARM INDS INC Discontinued
HYDROCHLOROTHIAZIDE 040907 001 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 25MG No No 2008/08/15 2008/08/15 UNICHEM Prescription
HYDROCHLOROTHIAZIDE 040907 002 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 50MG No No 2008/08/15 2008/08/15 UNICHEM Prescription
HYDROCHLOROTHIAZIDE 040907 003 ANDA HYDROCHLOROTHIAZIDE TABLET;ORAL 12.5MG No No 2008/08/15 2025/04/03 UNICHEM Prescription
MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 090096 001 ANDA HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE TABLET;ORAL 12.5MG;7.5MG No No 2008/09/25 2008/09/25 CHARTWELL RX Discontinued
MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 090096 002 ANDA HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE TABLET;ORAL 12.5MG;15MG No No 2008/09/25 2008/09/25 CHARTWELL RX Discontinued
MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 090096 003 ANDA HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE TABLET;ORAL 25MG;15MG No No 2008/09/25 2008/09/25 CHARTWELL RX Discontinued
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 078211 001 ANDA HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE TABLET;ORAL 12.5MG;EQ 10MG BASE No No 2009/03/04 2009/03/04 SUN PHARM INDS LTD Discontinued
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 078211 002 ANDA HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE TABLET;ORAL 12.5MG;EQ 20MG BASE No No 2009/03/04 2009/03/04 SUN PHARM INDS LTD Discontinued
QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 078211 003 ANDA HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE TABLET;ORAL 25MG;EQ 20MG BASE No No 2009/03/04 2009/03/04 SUN PHARM INDS LTD Discontinued
HYDROCHLOROTHIAZIDE 079237 001 ANDA HYDROCHLOROTHIAZIDE CAPSULE;ORAL 12.5MG No No 2009/04/02 2009/04/02 IPCA LABS LTD Discontinued
药品名称,活性成分,申请号搜索 高级检索
©2006-2025 DrugFuture->U.S. FDA Drugs Database