TEVA PHARMS USA FDA Approval ANDA 211272

ANDA 211272

TEVA PHARMS USA

FDA Drug Application

Application #211272

Application Sponsors

ANDA 211272TEVA PHARMS USA

Marketing Status

Prescription001

Application Products

001FOR SUSPENSION;ORAL200MG/ML0MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL

FDA Submissions

UNKNOWN; ORIG1AP2022-01-25STANDARD

Submissions Property Types

ORIG1Null7

TE Codes

001PrescriptionAB

CDER Filings

TEVA PHARMS USA
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 211272
            [companyName] => TEVA PHARMS USA
            [docInserts] => ["",""]
            [products] => [{"drugName":"MYCOPHENOLATE MOFETIL","activeIngredients":"MYCOPHENOLATE MOFETIL","strength":"200MG\/ML","dosageForm":"FOR SUSPENSION;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"01\/25\/2022","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2022-01-25
        )

)

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