PHARMACIA AND UPJOHN FDA Approval ANDA 081242

ANDA 081242

PHARMACIA AND UPJOHN

FDA Drug Application

Application #081242

Application Sponsors

ANDA 081242PHARMACIA AND UPJOHN

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTIONEQ 25MG BASE/ML0FOLEX PFSMETHOTREXATE SODIUM

FDA Submissions

ORIG1AP1991-08-23

CDER Filings

PHARMACIA AND UPJOHN
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 81242
            [companyName] => PHARMACIA AND UPJOHN
            [docInserts] => ["",""]
            [products] => [{"drugName":"FOLEX PFS","activeIngredients":"METHOTREXATE SODIUM","strength":"EQ 25MG BASE\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"FOLEX PFS","submission":"METHOTREXATE SODIUM","actionType":"EQ 25MG BASE\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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