NOVARTIS FDA Approval ANDA 074857

ANDA 074857

NOVARTIS

FDA Drug Application

Application #074857

Application Sponsors

ANDA 074857NOVARTIS

Marketing Status

Discontinued001

Application Products

001CAPSULE;ORAL25MG;37.5MG0TRIAMTERENE AND HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE; TRIAMTERENE

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 74857
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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