← FDA DRUG APPROVALS

FDA ANDA · ANDA078627

VENLAFAXINE

Sponsor: SUN PHARM INDS INC

APPLICATION
ANDA078627
TYPE
ANDA
ORIGINAL APPROVAL
2008-06-13
LATEST ACTION
2023-08-21
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription

Products

VENLAFAXINE HYDROCHLORIDEPrescription
VENLAFAXINE HYDROCHLORIDE EQ 25MG BASE · TABLET · ORAL
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

Approval history

2023-08-21Labeling · Supplement 15 · standardAP
2021-09-21Labeling · Supplement 14 · standardAP
2021-09-02Labeling · Supplement 12 · standardAP
2017-01-04Labeling · Supplement 11 · standardAP
2014-11-17Labeling · Supplement 10 · standardAP
2009-04-08Labeling · Supplement 2AP
2008-06-13OriginalAP
VIEW ON DRUGS@FDA ↗

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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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