PARKE DAVIS FDA Approval NDA 016749

NDA 016749

PARKE DAVIS

FDA Drug Application

Application #016749

Application Sponsors

NDA 016749PARKE DAVIS

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL-210.05MG;1MG0NORLESTRIN 21 1/50ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 16749
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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