MYLAN LABS LTD FDA Approval ANDA 203927

ANDA 203927

MYLAN LABS LTD

FDA Drug Application

Application #203927

Application Sponsors

ANDA 203927MYLAN LABS LTD

Marketing Status

Discontinued001
Discontinued002

Application Products

001INJECTABLE;INJECTIONEQ 500MG BASE/VIAL0ACYCLOVIR SODIUMACYCLOVIR SODIUM
002INJECTABLE;INJECTIONEQ 1GM BASE/VIAL0ACYCLOVIR SODIUMACYCLOVIR SODIUM

FDA Submissions

UNKNOWN; ORIG1AP2017-03-29

Submissions Property Types

ORIG1Null15

CDER Filings

MYLAN LABS LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 203927
            [companyName] => MYLAN LABS LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"ACYCLOVIR SODIUM","activeIngredients":"ACYCLOVIR SODIUM","strength":"EQ 500MG BASE\/VIAL","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"ACYCLOVIR SODIUM","activeIngredients":"ACYCLOVIR SODIUM","strength":"EQ 1GM BASE\/VIAL","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"03\/29\/2017","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2017-03-29
        )

)

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