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FDA ANDA · ANDA040857

HYDROCHLOROTHIAZIDE

Sponsor: SUN PHARM INDS INC

APPLICATION
ANDA040857
TYPE
ANDA
ORIGINAL APPROVAL
2008-05-30
LATEST ACTION
2020-08-20
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

HYDROCHLOROTHIAZIDEDiscontinued
HYDROCHLOROTHIAZIDE 12.5MG · TABLET · ORAL

Approval history

2020-08-20Labeling · Supplement 7 · standardAP
2008-05-30OriginalAP
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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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