美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=AMILORIDE HYDROCHLORIDE"
符合检索条件的记录共 8 条
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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
AMILORIDE HYDROCHLORIDE 070346 001 ANDA AMILORIDE HYDROCHLORIDE TABLET;ORAL 5MG No Yes 1986/01/22 1986/01/22 PAR PHARM Prescription
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 070795 001 ANDA AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL EQ 5MG ANHYDROUS;50MG No No 1987/07/15 1988/04/17 TEVA Discontinued
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 071111 001 ANDA AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE TABLET;ORAL EQ 5MG ANHYDROUS;50MG No No 1988/05/10 1988/05/10 BARR Prescription
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
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
AMILORIDE HYDROCHLORIDE 079133 001 ANDA AMILORIDE HYDROCHLORIDE TABLET;ORAL 5MG No No 2009/01/30 2009/01/30 SIGMAPHARM LABS LLC Prescription
AMILORIDE HYDROCHLORIDE 204180 001 ANDA AMILORIDE HYDROCHLORIDE TABLET;ORAL 5MG No No 2015/08/07 2015/08/07 CHARTWELL RX Discontinued
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