美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN"
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 Discontinued
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
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