APOTEX CORP FDA Approval ANDA 091379

ANDA 091379

APOTEX CORP

FDA Drug Application

Application #091379

Documents

Letter2012-11-07

Application Sponsors

ANDA 091379APOTEX CORP

Marketing Status

Discontinued001

Application Products

001TABLET;ORALEQ 20MG BASE0SILDENAFIL CITRATESILDENAFIL CITRATE

FDA Submissions

ORIG1AP2012-11-06
LABELING; LabelingSUPPL2AP2015-03-16STANDARD

Submissions Property Types

ORIG1Null15
SUPPL2Null15

CDER Filings

APOTEX CORP
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 91379
            [companyName] => APOTEX CORP
            [docInserts] => ["",""]
            [products] => [{"drugName":"SILDENAFIL CITRATE","activeIngredients":"SILDENAFIL CITRATE","strength":"EQ 20MG BASE","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"SILDENAFIL CITRATE","submission":"SILDENAFIL CITRATE","actionType":"EQ 20MG BASE","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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