NEXGEN PHARMA INC FDA Approval ANDA 084220

ANDA 084220

NEXGEN PHARMA INC

FDA Drug Application

Application #084220

Application Sponsors

ANDA 084220NEXGEN PHARMA INC

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL200MG0MEPROBAMATEMEPROBAMATE

FDA Submissions

ORIG1AP1974-09-30

CDER Filings

NEXGEN PHARMA INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 84220
            [companyName] => NEXGEN PHARMA INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"MEPROBAMATE","activeIngredients":"MEPROBAMATE","strength":"200MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"MEPROBAMATE","submission":"MEPROBAMATE","actionType":"200MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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