PARKE DAVIS FDA Approval NDA 018089

NDA 018089

PARKE DAVIS

FDA Drug Application

Application #018089

Application Sponsors

NDA 018089PARKE DAVIS

Marketing Status

Discontinued001

Application Products

001OINTMENT;TOPICAL0.025%0UTICORTBETAMETHASONE BENZOATE

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 18089
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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