AUROBINDO PHARMA LTD FDA Approval ANDA 215671

ANDA 215671

AUROBINDO PHARMA LTD

FDA Drug Application

Application #215671

Application Sponsors

ANDA 215671AUROBINDO PHARMA LTD

Marketing Status

Prescription001

Application Products

001TABLET;ORAL1MG0PREDNISONEPREDNISONE

FDA Submissions

UNKNOWN; ORIG1AP2021-11-16STANDARD

Submissions Property Types

ORIG1Null7

TE Codes

001PrescriptionAB

CDER Filings

AUROBINDO PHARMA LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 215671
            [companyName] => AUROBINDO PHARMA LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"PREDNISONE","activeIngredients":"PREDNISONE","strength":"1MG","dosageForm":"TABLET;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"11\/16\/2021","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2021-11-16
        )

)

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