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FDA ANDA · ANDA076459

QUINAPRIL HYDROCHLORIDE

Sponsor: ACTAVIS ELIZABETH

APPLICATION
ANDA076459
TYPE
ANDA
ORIGINAL APPROVAL
2004-12-22
LATEST ACTION
2006-03-17
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

QUINAPRIL HYDROCHLORIDEDiscontinued
QUINAPRIL HYDROCHLORIDE EQ 20MG BASE · TABLET · ORAL
QUINAPRIL HYDROCHLORIDEDiscontinued
QUINAPRIL HYDROCHLORIDE EQ 5MG BASE · TABLET · ORAL
QUINAPRIL HYDROCHLORIDEDiscontinued
QUINAPRIL HYDROCHLORIDE EQ 40MG BASE · TABLET · ORAL
QUINAPRIL HYDROCHLORIDEDiscontinued
QUINAPRIL HYDROCHLORIDE EQ 10MG BASE · TABLET · ORAL

Approval history

2006-03-17Labeling · Supplement 4AP
2004-12-22OriginalAP
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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