LANNETT CO INC FDA Approval ANDA 209221

ANDA 209221

LANNETT CO INC

FDA Drug Application

Application #209221

Application Sponsors

ANDA 209221LANNETT CO INC

Marketing Status

Discontinued001

Application Products

001CAPSULE;ORAL100MG0AMANTADINE HYDROCHLORIDEAMANTADINE HYDROCHLORIDE

FDA Submissions

UNKNOWN; ORIG1AP2017-06-15STANDARD

Submissions Property Types

ORIG1Null15

CDER Filings

LANNETT CO INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 209221
            [companyName] => LANNETT CO INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"AMANTADINE HYDROCHLORIDE","activeIngredients":"AMANTADINE HYDROCHLORIDE","strength":"100MG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"06\/15\/2017","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2017-06-15
        )

)

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