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FDA ANDA · ANDA201762

QUETIAPINE FUMARATE

Sponsor: ACTAVIS GRP PTC

APPLICATION
ANDA201762
TYPE
ANDA
ORIGINAL APPROVAL
2013-02-27
LATEST ACTION
2013-02-27
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

QUETIAPINE FUMARATEDiscontinued
QUETIAPINE FUMARATE EQ 400MG BASE · TABLET · ORAL
QUETIAPINE FUMARATEDiscontinued
QUETIAPINE FUMARATE EQ 200MG BASE · TABLET · ORAL
QUETIAPINE FUMARATEDiscontinued
QUETIAPINE FUMARATE EQ 100MG BASE · TABLET · ORAL
QUETIAPINE FUMARATEDiscontinued
QUETIAPINE FUMARATE EQ 25MG BASE · TABLET · ORAL
QUETIAPINE FUMARATEDiscontinued
QUETIAPINE FUMARATE EQ 300MG BASE · TABLET · ORAL
QUETIAPINE FUMARATEDiscontinued
QUETIAPINE FUMARATE EQ 150MG BASE · TABLET · ORAL
QUETIAPINE FUMARATEDiscontinued
QUETIAPINE FUMARATE EQ 50MG BASE · TABLET · ORAL

Approval history

2013-02-27Not Applicable · OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industry →GMP discipline →FDA drug shortages →FDA enforcement & recalls →

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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