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FDA ANDA · ANDA090555
VENLAFAXINE
venlafaxine hydrochloride
Sponsor: AUROBINDO PHARMA
APPLICATION
ANDA090555
TYPE
ANDA
ORIGINAL APPROVAL
2010-04-07
LATEST ACTION
2023-08-18
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription
Products
VENLAFAXINE HYDROCHLORIDEPrescription
VENLAFAXINE HYDROCHLORIDE EQ 75MG BASE · TABLET · ORAL
VENLAFAXINE HYDROCHLORIDEPrescription
VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE · TABLET · ORAL
VENLAFAXINE HYDROCHLORIDEPrescription
VENLAFAXINE HYDROCHLORIDE EQ 100MG BASE · TABLET · ORAL
VENLAFAXINE HYDROCHLORIDEPrescription
VENLAFAXINE HYDROCHLORIDE EQ 50MG BASE · TABLET · ORAL
VENLAFAXINE HYDROCHLORIDEPrescription
VENLAFAXINE HYDROCHLORIDE EQ 25MG BASE · TABLET · ORAL
Approval history
2023-08-18Labeling · Supplement 24 · standardAP
2021-09-20Labeling · Supplement 19 · standardAP
2020-04-14Labeling · Supplement 15 · standardAP
2017-01-04Labeling · Supplement 13 · standardAP
2014-07-17Labeling · Supplement 9 · standardAP
2014-06-18Labeling · Supplement 6 · standardAP
2012-09-19Labeling · Supplement 4 · standardAP
2010-04-07OriginalAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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