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FDA ANDA · ANDA076739

FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

Sponsor: SUN PHARM INDS LTD

APPLICATION
ANDA076739
TYPE
ANDA
ORIGINAL APPROVAL
2004-12-17
LATEST ACTION
2009-11-06
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDEDiscontinued
FOSINOPRIL SODIUM 10MG, HYDROCHLOROTHIAZIDE 12.5MG · TABLET · ORAL
FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDEDiscontinued
FOSINOPRIL SODIUM 20MG, HYDROCHLOROTHIAZIDE 12.5MG · TABLET · ORAL

Approval history

2009-11-06Labeling · Supplement 4AP
2004-12-17OriginalAP
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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