NOVARTIS FDA Approval ANDA 086765

ANDA 086765

NOVARTIS

FDA Drug Application

Application #086765

Application Sponsors

ANDA 086765NOVARTIS

Marketing Status

Discontinued001

Application Products

001CONCENTRATE;ORAL25MG/ML0IMIPRAMINE HYDROCHLORIDEIMIPRAMINE HYDROCHLORIDE

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 86765
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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