美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=OXYCODONE HYDROCHLORIDE"
符合检索条件的记录共 123 条
共 7 页，当前第 2 页
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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
OXYCODONE HYDROCHLORIDE 077290 005 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 30MG No No 2005/12/08 2005/12/08 NESHER PHARMS Discontinued
OXYCODONE HYDROCHLORIDE 077712 001 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 15MG No No 2007/01/31 2007/01/31 STRIDES PHARMA Discontinued
OXYCODONE HYDROCHLORIDE 077712 002 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 30MG No No 2007/01/31 2007/01/31 STRIDES PHARMA Discontinued
OXYCODONE HYDROCHLORIDE 077712 003 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 5MG No No 2007/01/31 2009/03/02 STRIDES PHARMA Discontinued
OXYCODONE HYDROCHLORIDE 077712 004 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 10MG No No 2007/01/31 2015/04/13 STRIDES PHARMA Discontinued
OXYCODONE HYDROCHLORIDE 077712 005 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 20MG No No 2007/01/31 2015/04/13 STRIDES PHARMA Discontinued
OXYCODONE HYDROCHLORIDE AND IBUPROFEN 078394 001 ANDA IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET;ORAL 400MG;5MG No No 2007/11/26 2007/11/26 WATSON LABS Discontinued
OXYCODONE HYDROCHLORIDE AND IBUPROFEN 078316 001 ANDA IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET;ORAL 400MG;5MG No No 2007/11/29 2007/11/29 BARR LABS INC Discontinued
OXYCODONE HYDROCHLORIDE AND IBUPROFEN 078769 001 ANDA IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET;ORAL 400MG;5MG No No 2008/01/04 2008/01/04 ACTAVIS ELIZABETH Discontinued
OXYCODONE HYDROCHLORIDE 077822 001 ANDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE; ORAL 10MG No No 2008/07/24 -- MALLINCKRODT None (Tentative Approval)
OXYCODONE HYDROCHLORIDE 077822 002 ANDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE; ORAL 20MG No No 2008/07/24 -- MALLINCKRODT None (Tentative Approval)
OXYCODONE HYDROCHLORIDE 077822 003 ANDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE; ORAL 40MG No No 2008/07/24 -- MALLINCKRODT None (Tentative Approval)
OXYCODONE HYDROCHLORIDE 077822 004 ANDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE; ORAL 80MG No No 2008/07/24 -- MALLINCKRODT None (Tentative Approval)
OXYCODONE HYDROCHLORIDE 090659 001 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 5MG No No 2009/04/10 2009/04/10 SUN PHARM INDS INC Prescription
OXYCODONE HYDROCHLORIDE 090659 002 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 15MG No No 2009/04/10 2009/04/10 SUN PHARM INDS INC Prescription
OXYCODONE HYDROCHLORIDE 090659 003 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 30MG No No 2009/04/10 2009/04/10 SUN PHARM INDS INC Prescription
OXYCODONE HYDROCHLORIDE 090659 004 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 20MG No No 2009/04/10 2012/11/06 SUN PHARM INDS INC Prescription
OXYCODONE HYDROCHLORIDE 090659 005 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 10MG No No 2009/04/10 2012/11/06 SUN PHARM INDS INC Prescription
OXYCODONE HYDROCHLORIDE 090895 001 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 5MG No No 2009/08/24 2009/08/24 EPIC PHARMA LLC Prescription
OXYCODONE HYDROCHLORIDE 090895 002 ANDA OXYCODONE HYDROCHLORIDE TABLET;ORAL 15MG No No 2009/08/24 2009/08/24 EPIC PHARMA LLC Prescription
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