MORTON GROVE FDA Approval ANDA 088242

ANDA 088242

MORTON GROVE

FDA Drug Application

Application #088242

Application Sponsors

ANDA 088242MORTON GROVE

Marketing Status

Discontinued001

Application Products

001SYRUP;ORAL50MG/5ML0OXTRIPHYLLINE PEDIATRICOXTRIPHYLLINE

CDER Filings

MORTON GROVE
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 88242
            [companyName] => MORTON GROVE
            [docInserts] => ["",""]
            [products] => [{"drugName":"OXTRIPHYLLINE PEDIATRIC","activeIngredients":"OXTRIPHYLLINE","strength":"50MG\/5ML","dosageForm":"SYRUP;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"OXTRIPHYLLINE PEDIATRIC","submission":"OXTRIPHYLLINE","actionType":"50MG\/5ML","submissionClassification":"SYRUP;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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