AKORN FDA Approval ANDA 087519

ANDA 087519

AKORN

FDA Drug Application

Application #087519

Application Sponsors

ANDA 087519AKORN

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION100MG/ML0NANDROLONE DECANOATENANDROLONE DECANOATE

CDER Filings

AKORN
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 87519
            [companyName] => AKORN
            [docInserts] => ["",""]
            [products] => [{"drugName":"NANDROLONE DECANOATE","activeIngredients":"NANDROLONE DECANOATE","strength":"100MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"NANDROLONE DECANOATE","submission":"NANDROLONE DECANOATE","actionType":"100MG\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.