NDA 022244

EISAI INC

FDA Drug Application

Application #022244

Application Sponsors

NDA 022244

EISAI INC

Marketing Status

• Discontinued: 001

Application Products

001

SOLUTION;INTRAVENOUS

1050MG/30ML (35MG/ML)

0

LUSEDRA

FOSPROPOFOL DISODIUM

FDA Submissions

TYPE 1; Type 1 - New Molecular Entity

ORIG

1

AP

2008-12-08

STANDARD

CDER Filings

EISAI INC

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 22244
            [companyName] => EISAI INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"LUSEDRA","activeIngredients":"FOSPROPOFOL DISODIUM","strength":"1050MG\/30ML (35MG\/ML)","dosageForm":"SOLUTION;INTRAVENOUS","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"LUSEDRA","submission":"FOSPROPOFOL DISODIUM","actionType":"1050MG\/30ML (35MG\/ML)","submissionClassification":"SOLUTION;INTRAVENOUS","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)