LILLY FDA Approval ANDA 085103

ANDA 085103

LILLY

FDA Drug Application

Application #085103

Application Sponsors

ANDA 085103LILLY

Marketing Status

Discontinued001

Application Products

001CAPSULE;ORAL200MG0QUINIDINE SULFATEQUINIDINE SULFATE

FDA Submissions

ORIG1AP1976-07-08
LABELING; LabelingSUPPL7AP1991-03-15

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 85103
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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