NEXGEN PHARMA INC FDA Approval ANDA 084238

ANDA 084238

NEXGEN PHARMA INC

FDA Drug Application

Application #084238

Application Sponsors

ANDA 084238NEXGEN PHARMA INC

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL100MG0SODIUM PENTOBARBITALPENTOBARBITAL SODIUM

FDA Submissions

ORIG1AP1974-09-23

CDER Filings

NEXGEN PHARMA INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 84238
            [companyName] => NEXGEN PHARMA INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"SODIUM PENTOBARBITAL","activeIngredients":"PENTOBARBITAL SODIUM","strength":"100MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"SODIUM PENTOBARBITAL","submission":"PENTOBARBITAL SODIUM","actionType":"100MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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