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FDA ANDA · ANDA078789

VENLAFAXINE HYDROCHLORIDE

Sponsor: PHARMOBEDIENT

APPLICATION
ANDA078789
TYPE
ANDA
ORIGINAL APPROVAL
2011-06-01
LATEST ACTION
2024-05-31
ROUTE
ORAL
DOSAGE FORM
CAPSULE, EXTENDED RELEASE
MARKETING STATUS
Discontinued

Products

VENLAFAXINE HYDROCHLORIDEDiscontinued
VENLAFAXINE HYDROCHLORIDE EQ 75MG BASE · CAPSULE, EXTENDED RELEASE · ORAL
VENLAFAXINE HYDROCHLORIDEDiscontinued
VENLAFAXINE HYDROCHLORIDE EQ 150MG BASE · CAPSULE, EXTENDED RELEASE · ORAL
VENLAFAXINE HYDROCHLORIDEDiscontinued
VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE · CAPSULE, EXTENDED RELEASE · ORAL

Approval history

2024-05-31Labeling · Supplement 12 · standardAP
2023-06-06Labeling · Supplement 10 · standardAP
2023-06-06Labeling · Supplement 7 · standardAP
2023-06-06Labeling · Supplement 11 · standardAP
2023-06-06Labeling · Supplement 8 · standardAP
2015-10-02Labeling · Supplement 6 · standardAP
2014-01-29Labeling · Supplement 4 · standardAP
2014-01-29Labeling · Supplement 2 · standardAP
2011-06-01OriginalReviewAP
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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