SANOFI AVENTIS US FDA Approval ANDA 085264

ANDA 085264

SANOFI AVENTIS US

FDA Drug Application

Application #085264

Application Sponsors

ANDA 085264SANOFI AVENTIS US

Marketing Status

Discontinued001
Discontinued002

Application Products

001CAPSULE;ORAL100MG0BRONKODYLTHEOPHYLLINE
002CAPSULE;ORAL200MG0BRONKODYLTHEOPHYLLINE

CDER Filings

SANOFI AVENTIS US
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 85264
            [companyName] => SANOFI AVENTIS US
            [docInserts] => ["",""]
            [products] => [{"drugName":"BRONKODYL","activeIngredients":"THEOPHYLLINE","strength":"100MG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"BRONKODYL","activeIngredients":"THEOPHYLLINE","strength":"200MG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"BRONKODYL","submission":"THEOPHYLLINE","actionType":"100MG","submissionClassification":"CAPSULE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"BRONKODYL","submission":"THEOPHYLLINE","actionType":"200MG","submissionClassification":"CAPSULE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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