SANOFI AVENTIS US FDA Approval ANDA 083517

ANDA 083517

SANOFI AVENTIS US

FDA Drug Application

Application #083517

Application Sponsors

ANDA 083517SANOFI AVENTIS US

Marketing Status

Discontinued001

Application Products

001SUPPOSITORY;VAGINAL0.7MG0DVDIENESTROL

CDER Filings

SANOFI AVENTIS US
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 83517
            [companyName] => SANOFI AVENTIS US
            [docInserts] => ["",""]
            [products] => [{"drugName":"DV","activeIngredients":"DIENESTROL","strength":"0.7MG","dosageForm":"SUPPOSITORY;VAGINAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"DV","submission":"DIENESTROL","actionType":"0.7MG","submissionClassification":"SUPPOSITORY;VAGINAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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