美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=NALTREXONE HYDROCHLORIDE"
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
NALTREXONE HYDROCHLORIDE 074918 001 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 50MG No No 1998/05/08 1998/05/08 BARR Prescription
NALTREXONE HYDROCHLORIDE 075274 001 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 50MG No No 1999/05/26 1999/05/26 ELITE LABS Prescription
NALTREXONE HYDROCHLORIDE 075434 001 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 50MG No No 2000/03/08 2000/03/08 FOSUN PHARMA Discontinued
NALTREXONE HYDROCHLORIDE 076264 001 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 25MG No No 2002/03/22 2002/03/22 SPECGX LLC Prescription
NALTREXONE HYDROCHLORIDE 076264 002 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 50MG No Yes 2002/03/22 2002/03/22 SPECGX LLC Prescription
NALTREXONE HYDROCHLORIDE 076264 003 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 100MG No No 2002/03/22 2002/03/22 SPECGX LLC Prescription
NALTREXONE HYDROCHLORIDE 091205 001 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 50MG No No 2011/08/17 2011/08/17 ACCORD HLTHCARE Prescription
NALTREXONE HYDROCHLORIDE 090356 001 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 50MG No No 2012/02/24 2012/02/24 SUN PHARM Prescription
NALTREXONE HYDROCHLORIDE 207905 001 ANDA NALTREXONE HYDROCHLORIDE TABLET;ORAL 50MG No No 2017/07/21 2017/07/21 CHARTWELL Prescription
NALTREXONE HYDROCHLORIDE; BUPROPION HYDROCHLORIDE 208043 001 ANDA NALTREXONE HYDROCHLORIDE;BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE; ORAL 8MG/90MG No No 2022/11/29 (TA) -- ACTAVIS LABS FL INC None (Tentative Approval)
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