SANOFI AVENTIS US FDA Approval NDA 018237

NDA 018237

SANOFI AVENTIS US

FDA Drug Application

Application #018237

Application Sponsors

NDA 018237SANOFI AVENTIS US

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION25,000 UNITS/ML0CALCIPARINEHEPARIN CALCIUM

CDER Filings

SANOFI AVENTIS US
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 18237
            [companyName] => SANOFI AVENTIS US
            [docInserts] => ["",""]
            [products] => [{"drugName":"CALCIPARINE","activeIngredients":"HEPARIN CALCIUM","strength":"25,000 UNITS\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"CALCIPARINE","submission":"HEPARIN CALCIUM","actionType":"25,000 UNITS\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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