HIKMA FDA Approval ANDA 214334

ANDA 214334

HIKMA

FDA Drug Application

Application #214334

Application Sponsors

ANDA 214334HIKMA

Marketing Status

Prescription001

Application Products

001SOLUTION;INTRAVENOUS50MG/ML (50MG/ML)0EPHEDRINE SULFATEEPHEDRINE SULFATE

FDA Submissions

UNKNOWN; ORIG1AP2020-12-15STANDARD

Submissions Property Types

ORIG1Null7

TE Codes

001PrescriptionAP

CDER Filings

HIKMA
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 214334
            [companyName] => HIKMA
            [docInserts] => ["",""]
            [products] => [{"drugName":"EPHEDRINE SULFATE","activeIngredients":"EPHEDRINE SULFATE","strength":"50MG\/ML (50MG\/ML)","dosageForm":"SOLUTION;INTRAVENOUS","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"12\/15\/2020","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2020-12-15
        )

)

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