ORGANON USA INC FDA Approval NDA 014006

NDA 014006

ORGANON USA INC

FDA Drug Application

Application #014006

Application Sponsors

NDA 014006ORGANON USA INC

Marketing Status

Discontinued002

Application Products

002ELIXIR;ORAL2MG/5ML0MAXIBOLINETHYLESTRENOL

FDA Submissions

TYPE 3; Type 3 - New Dosage FormORIG1AP1965-01-07STANDARD

CDER Filings

ORGANON USA INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 14006
            [companyName] => ORGANON USA INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"MAXIBOLIN","activeIngredients":"ETHYLESTRENOL","strength":"2MG\/5ML","dosageForm":"ELIXIR;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"MAXIBOLIN","submission":"ETHYLESTRENOL","actionType":"2MG\/5ML","submissionClassification":"ELIXIR;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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