美国FDA药品数据库-药物在线

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
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	209281	003	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	25MG;40MG	No	No	2019/02/07	2019/02/07	ACCORD HLTHCARE	Prescription
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	208847	001	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	12.5MG;20MG	No	No	2019/09/17	2019/09/17	UMEDICA	Prescription
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	208847	002	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	25MG;40MG	No	No	2019/09/17	2019/09/17	UMEDICA	Prescription
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	208847	003	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	12.5MG;40MG	No	No	2019/09/17	2019/09/17	UMEDICA	Prescription
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	206377	001	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	12.5MG;20MG	No	No	2023/02/24	2023/02/24	ZYDUS PHARMS	Discontinued
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	206377	002	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	12.5MG;40MG	No	No	2023/02/24	2023/02/24	ZYDUS PHARMS	Discontinued
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	206377	003	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	25MG;40MG	No	No	2023/02/24	2023/02/24	ZYDUS PHARMS	Discontinued
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	204801	001	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	12.5MG;20MG	No	No	2023/06/01	2023/06/01	MACLEODS PHARMS LTD	Prescription
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	204801	002	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	12.5MG;40MG	No	No	2023/06/01	2023/06/01	MACLEODS PHARMS LTD	Prescription
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	204801	003	ANDA	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	TABLET;ORAL	25MG;40MG	No	No	2023/06/01	2023/06/01	MACLEODS PHARMS LTD	Prescription