SANOFI AVENTIS US FDA Approval ANDA 088746

ANDA 088746

SANOFI AVENTIS US

FDA Drug Application

Application #088746

Application Sponsors

ANDA 088746SANOFI AVENTIS US

Marketing Status

Discontinued001

Application Products

001SYRUP;ORAL150MG/15ML0ACCURBRONTHEOPHYLLINE

CDER Filings

SANOFI AVENTIS US
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 88746
            [companyName] => SANOFI AVENTIS US
            [docInserts] => ["",""]
            [products] => [{"drugName":"ACCURBRON","activeIngredients":"THEOPHYLLINE","strength":"150MG\/15ML","dosageForm":"SYRUP;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"ACCURBRON","submission":"THEOPHYLLINE","actionType":"150MG\/15ML","submissionClassification":"SYRUP;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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