ABBOTT FDA Approval NDA 018923

NDA 018923

ABBOTT

FDA Drug Application

Application #018923

Application Sponsors

NDA 018923ABBOTT

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION38.5GM/100ML0DEXTROSE 38.5% IN PLASTIC CONTAINERDEXTROSE

CDER Filings

ABBOTT
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 18923
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"DEXTROSE 38.5% IN PLASTIC CONTAINER","activeIngredients":"DEXTROSE","strength":"38.5GM\/100ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"DEXTROSE 38.5% IN PLASTIC CONTAINER","submission":"DEXTROSE","actionType":"38.5GM\/100ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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