AKORN FDA Approval ANDA 203787

ANDA 203787

AKORN

FDA Drug Application

Application #203787

Application Sponsors

ANDA 203787AKORN

Marketing Status

Prescription001

Application Products

001CREAM;TOPICAL0.05%0DESOXIMETASONEDESOXIMETASONE

FDA Submissions

UNKNOWN; ORIG1AP2017-01-06

Submissions Property Types

ORIG1Null17

TE Codes

001PrescriptionAB

CDER Filings

AKORN
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 203787
            [companyName] => AKORN
            [docInserts] => ["",""]
            [products] => [{"drugName":"DESOXIMETASONE","activeIngredients":"DESOXIMETASONE","strength":"0.05%","dosageForm":"CREAM;TOPICAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"01\/06\/2017","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2017-01-06
        )

)

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