ABBOTT FDA Approval ANDA 089575

ANDA 089575

ABBOTT

FDA Drug Application

Application #089575

Application Sponsors

ANDA 089575ABBOTT

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTIONEQ 500MG BASE/VIAL0A-METHAPREDMETHYLPREDNISOLONE SODIUM SUCCINATE

FDA Submissions

ORIG1AP1991-02-22
MANUF (CMC); Manufacturing (CMC)SUPPL2AP2002-03-12

Submissions Property Types

ORIG1Null0
SUPPL2Null0

CDER Filings

ABBOTT
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 89575
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"A-METHAPRED","activeIngredients":"METHYLPREDNISOLONE SODIUM SUCCINATE","strength":"EQ 500MG BASE\/VIAL","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"A-METHAPRED","submission":"METHYLPREDNISOLONE SODIUM SUCCINATE","actionType":"EQ 500MG BASE\/VIAL","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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