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FDA ANDA · ANDA089137

SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE

Sponsor: SUPERPHARM

APPLICATION
ANDA089137
TYPE
ANDA
ORIGINAL APPROVAL
1985-08-26
LATEST ACTION
1989-07-24
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

SPIRONOLACTONE AND HYDROCHLOROTHIAZIDEDiscontinued
HYDROCHLOROTHIAZIDE 25MG, SPIRONOLACTONE 25MG · TABLET · ORAL

Approval history

1989-07-24Labeling · Supplement 7AP
1985-08-26OriginalAP
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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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