PARKE DAVIS FDA Approval NDA 010962

NDA 010962

PARKE DAVIS

FDA Drug Application

Application #010962

Application Sponsors

NDA 010962PARKE DAVIS

Marketing Status

Discontinued002

Application Products

002TABLET;ORAL5MG0PARACORTPREDNISONE

FDA Submissions

LABELING; LabelingSUPPL7AP1978-07-13
MANUF (CMC); Manufacturing (CMC)SUPPL9AP1980-05-06STANDARD

Submissions Property Types

SUPPL9Null0

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 10962
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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