PARKE DAVIS FDA Approval ANDA 062231

ANDA 062231

PARKE DAVIS

FDA Drug Application

Application #062231

Application Sponsors

ANDA 062231PARKE DAVIS

Marketing Status

Discontinued001
Discontinued002

Application Products

001SUSPENSION;ORALEQ 200MG BASE/5ML0ERYTHROMYCIN ETHYLSUCCINATEERYTHROMYCIN ETHYLSUCCINATE
002SUSPENSION;ORALEQ 400MG BASE/5ML0ERYTHROMYCIN ETHYLSUCCINATEERYTHROMYCIN ETHYLSUCCINATE

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 62231
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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