UCB INC FDA Approval ANDA 085171

ANDA 085171

UCB INC

FDA Drug Application

Application #085171

Application Sponsors

ANDA 085171UCB INC

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL500MG0GLUTETHIMIDEGLUTETHIMIDE

CDER Filings

UCB INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 85171
            [companyName] => UCB INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"GLUTETHIMIDE","activeIngredients":"GLUTETHIMIDE","strength":"500MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"GLUTETHIMIDE","submission":"GLUTETHIMIDE","actionType":"500MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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