美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=AFAXIN"
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
VENLAFAXINE HYDROCHLORIDE 217767 001 ANDA VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE No No 2024/06/06 2024/06/06 ALEMBIC Prescription
VENLAFAXINE HYDROCHLORIDE 217767 002 ANDA VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE No No 2024/06/06 2024/06/06 ALEMBIC Prescription
VENLAFAXINE HYDROCHLORIDE 217767 003 ANDA VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE No No 2024/06/06 2024/06/06 ALEMBIC Prescription
DESVENLAFAXINE SUCCINATE 211427 001 ANDA DESVENLAFAXINE SUCCINATE TABLET, EXTENDED RELEASE;ORAL EQ 50MG BASE No No 2025/01/15 2025/01/15 MACLEODS PHARMS LTD Prescription
DESVENLAFAXINE SUCCINATE 211427 002 ANDA DESVENLAFAXINE SUCCINATE TABLET, EXTENDED RELEASE;ORAL EQ 100MG BASE No No 2025/01/15 2025/01/15 MACLEODS PHARMS LTD Prescription
VENLAFAXINE HYDROCHLORIDE 218180 001 ANDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 37.5MG BASE No No 2025/01/28 2025/01/28 TORRENT Prescription
VENLAFAXINE HYDROCHLORIDE 218180 002 ANDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 75MG BASE No No 2025/01/28 2025/01/28 TORRENT Prescription
VENLAFAXINE HYDROCHLORIDE 218180 003 ANDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 150MG BASE No No 2025/01/28 2025/01/28 TORRENT Prescription
VENLAFAXINE HYDROCHLORIDE 218180 004 ANDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 225MG BASE No No 2025/01/28 2025/01/28 TORRENT Prescription
VENLAFAXINE HYDROCHLORIDE 217841 001 ANDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 150MG BASE No No 2025/02/07 2025/02/07 ABON PHARMS LLC Prescription
VENLAFAXINE HYDROCHLORIDE 217841 002 ANDA VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 225MG BASE No No 2025/02/07 2025/02/07 ABON PHARMS LLC Prescription
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