美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=AFAXIN"
符合检索条件的记录共 203 条
共 11 页，当前第 1 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
AFAXIN 083187 001 ANDA VITAMIN A PALMITATE CAPSULE;ORAL EQ 50,000 UNITS BASE No No 1972/11/17 Approved Prior to Jan 1, 1982 STERLING WINTHROP Discontinued
VENLAFAXINE HYDROCHLORIDE 076690 001 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 25MG BASE No No 2006/08/03 2006/08/03 TEVA Prescription
VENLAFAXINE HYDROCHLORIDE 076690 002 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 37.5MG BASE No No 2006/08/03 2006/08/03 TEVA Prescription
VENLAFAXINE HYDROCHLORIDE 076690 003 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 50MG BASE No Yes 2006/08/03 2006/08/03 TEVA Prescription
VENLAFAXINE HYDROCHLORIDE 076690 004 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 75MG BASE No No 2006/08/03 2006/08/03 TEVA Prescription
VENLAFAXINE HYDROCHLORIDE 076690 005 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 100MG BASE No No 2006/08/03 2006/08/03 TEVA Prescription
VENLAFAXINE HYDROCHLORIDE 078517 001 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 25MG BASE No No 2007/06/25 (TA) 2008/06/13 PLIVA HRVATSKA DOO Discontinued
VENLAFAXINE HYDROCHLORIDE 078517 002 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 37.5MG BASE No No 2007/06/25 (TA) 2008/06/13 PLIVA HRVATSKA DOO Discontinued
VENLAFAXINE HYDROCHLORIDE 078517 003 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 50MG BASE No No 2007/06/25 (TA) 2008/06/13 PLIVA HRVATSKA DOO Discontinued
VENLAFAXINE HYDROCHLORIDE 078517 004 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 75MG BASE No No 2007/06/25 (TA) 2008/06/13 PLIVA HRVATSKA DOO Discontinued
VENLAFAXINE HYDROCHLORIDE 078517 005 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 100MG BASE No No 2007/06/25 (TA) 2008/06/13 PLIVA HRVATSKA DOO Discontinued
VENLAFAXINE HYDROCHLORIDE 078057 001 ANDA VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE; ORAL 37.5MG No No 2007/10/16 (TA) -- IMPAX LABS None (Tentative Approval)
VENLAFAXINE HYDROCHLORIDE 078057 002 ANDA VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE; ORAL 75MG No No 2007/10/16 (TA) -- IMPAX LABS None (Tentative Approval)
VENLAFAXINE HYDROCHLORIDE 078057 003 ANDA VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE; ORAL 150MG No No 2007/10/16 (TA) -- IMPAX LABS None (Tentative Approval)
VENLAFAXINE HYDROCHLORIDE 022104 001 NDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Yes No 2008/05/20 2008/05/20 OSMOTICA PHARM US Prescription
VENLAFAXINE HYDROCHLORIDE 022104 002 NDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 75MG BASE Yes No 2008/05/20 2008/05/20 OSMOTICA PHARM US Prescription
VENLAFAXINE HYDROCHLORIDE 022104 003 NDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 150MG BASE Yes Yes 2008/05/20 2008/05/20 OSMOTICA PHARM US Prescription
VENLAFAXINE HYDROCHLORIDE 022104 004 NDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 225MG BASE Yes No 2008/05/20 2008/05/20 OSMOTICA PHARM US Prescription
VENLAFAXINE HYDROCHLORIDE 077166 001 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 25MG BASE No No 2008/06/13 2008/06/13 NORVIUM BIOSCIENCE Discontinued
VENLAFAXINE HYDROCHLORIDE 077166 002 ANDA VENLAFAXINE HYDROCHLORIDE TABLET;ORAL EQ 37.5MG BASE No No 2008/06/13 2008/06/13 NORVIUM BIOSCIENCE Discontinued
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