SANOFI AVENTIS US FDA Approval ANDA 085206

ANDA 085206

SANOFI AVENTIS US

FDA Drug Application

Application #085206

Application Sponsors

ANDA 085206SANOFI AVENTIS US

Marketing Status

Discontinued001

Application Products

001CAPSULE, EXTENDED RELEASE;ORAL60MG0SLO-PHYLLINTHEOPHYLLINE

CDER Filings

SANOFI AVENTIS US
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 85206
            [companyName] => SANOFI AVENTIS US
            [docInserts] => ["",""]
            [products] => [{"drugName":"SLO-PHYLLIN","activeIngredients":"THEOPHYLLINE","strength":"60MG","dosageForm":"CAPSULE, EXTENDED RELEASE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"SLO-PHYLLIN","submission":"THEOPHYLLINE","actionType":"60MG","submissionClassification":"CAPSULE, EXTENDED RELEASE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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