LILLY FDA Approval ANDA 085038

ANDA 085038

LILLY

FDA Drug Application

Application #085038

Application Sponsors

ANDA 085038LILLY

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL200MG0QUINIDINE SULFATEQUINIDINE SULFATE

FDA Submissions

ORIG1AP1976-07-08

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 85038
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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