NEXGEN PHARMA INC FDA Approval ANDA 086020

ANDA 086020

NEXGEN PHARMA INC

FDA Drug Application

Application #086020

Application Sponsors

ANDA 086020NEXGEN PHARMA INC

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL35MG0PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE

FDA Submissions

ORIG1AP1978-02-28

CDER Filings

NEXGEN PHARMA INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 86020
            [companyName] => NEXGEN PHARMA INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"PHENDIMETRAZINE TARTRATE","activeIngredients":"PHENDIMETRAZINE TARTRATE","strength":"35MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"PHENDIMETRAZINE TARTRATE","submission":"PHENDIMETRAZINE TARTRATE","actionType":"35MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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