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FDA ANDA · ANDA076476

BENAZEPRIL HYDROCHLORIDE

Sponsor: GENPHARM

APPLICATION
ANDA076476
TYPE
ANDA
ORIGINAL APPROVAL
2004-02-11
LATEST ACTION
2004-02-11
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

BENAZEPRIL HYDROCHLORIDEDiscontinued
BENAZEPRIL HYDROCHLORIDE 40MG · TABLET · ORAL
BENAZEPRIL HYDROCHLORIDEDiscontinued
BENAZEPRIL HYDROCHLORIDE 10MG · TABLET · ORAL
BENAZEPRIL HYDROCHLORIDEDiscontinued
BENAZEPRIL HYDROCHLORIDE 20MG · TABLET · ORAL
BENAZEPRIL HYDROCHLORIDEDiscontinued
BENAZEPRIL HYDROCHLORIDE 5MG · TABLET · ORAL

Approval history

2004-02-11Original — Letter ↗AP
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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