HIKMA FDA Approval ANDA 202652

ANDA 202652

HIKMA

FDA Drug Application

Application #202652

Application Sponsors

ANDA 202652HIKMA

Marketing Status

Discontinued001
Discontinued002

Application Products

001TABLET;ORAL250MG0DISULFIRAMDISULFIRAM
002TABLET;ORAL500MG0DISULFIRAMDISULFIRAM

FDA Submissions

UNKNOWN; ORIG1AP2014-02-05

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAB
002PrescriptionAB

CDER Filings

HIKMA
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 202652
            [companyName] => HIKMA
            [docInserts] => ["",""]
            [products] => [{"drugName":"DISULFIRAM","activeIngredients":"DISULFIRAM","strength":"250MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"DISULFIRAM","activeIngredients":"DISULFIRAM","strength":"500MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"02\/05\/2014","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2014-02-05
        )

)

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