ACTAVIS LABS FL INC FDA Approval ANDA 075990

ANDA 075990

ACTAVIS LABS FL INC

FDA Drug Application

Application #075990

Application Sponsors

ANDA 075990ACTAVIS LABS FL INC

Marketing Status

Discontinued001

Application Products

001TABLET, ORALLY DISINTEGRATING;ORAL10MG0LORATADINELORATADINE

FDA Submissions

ORIG1AP2003-11-03

CDER Filings

ACTAVIS LABS FL INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 75990
            [companyName] => ACTAVIS LABS FL INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"LORATADINE","activeIngredients":"LORATADINE","strength":"10MG","dosageForm":"TABLET, ORALLY DISINTEGRATING;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"LORATADINE","submission":"LORATADINE","actionType":"10MG","submissionClassification":"TABLET, ORALLY DISINTEGRATING;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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