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
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	076475	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2005/04/21	2005/04/21	CHARTWELL RX	Discontinued
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	077184	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2005/12/16	2005/12/16	SUN PHARM INDS INC	Prescription
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	076914	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2006/07/26	2006/07/26	GRAVITI PHARMS	Discontinued
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	077858	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2008/09/26	2008/09/26	RISING	Prescription
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	090485	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	Yes	2009/12/09	2009/12/09	AMNEAL PHARMS	Prescription
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	202076	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2012/03/30	2012/03/30	ALKEM LABS LTD	Prescription
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	090460	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2012/09/06	2012/09/06	ZYDUS PHARMS USA INC	Prescription
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	201952	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2012/12/14	2012/12/14	MICRO LABS LTD INDIA	Prescription
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	078778	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2014/04/07	2014/04/07	NOSTRUM LABS INC	Discontinued
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	207152	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2017/03/22	2017/03/22	AUROBINDO PHARMA	Prescription
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	206885	001	ANDA	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	TABLET;ORAL	325MG;37.5MG	No	No	2017/05/02	2017/05/02	MACLEODS PHARMS LTD	Discontinued