PHARMACIA AND UPJOHN FDA Approval ANDA 088954

ANDA 088954

PHARMACIA AND UPJOHN

FDA Drug Application

Application #088954

Application Sponsors

ANDA 088954PHARMACIA AND UPJOHN

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTIONEQ 250MG BASE/VIAL0FOLEXMETHOTREXATE SODIUM

CDER Filings

PHARMACIA AND UPJOHN
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 88954
            [companyName] => PHARMACIA AND UPJOHN
            [docInserts] => ["",""]
            [products] => [{"drugName":"FOLEX","activeIngredients":"METHOTREXATE SODIUM","strength":"EQ 250MG BASE\/VIAL","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"FOLEX","submission":"METHOTREXATE SODIUM","actionType":"EQ 250MG BASE\/VIAL","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.