VISTAPHARM FDA Approval ANDA 213951

ANDA 213951

VISTAPHARM

FDA Drug Application

Application #213951

Application Sponsors

ANDA 213951VISTAPHARM

Marketing Status

Prescription001

Application Products

001SUSPENSION;ORAL200MG/5ML0ACYCLOVIRACYCLOVIR

FDA Submissions

UNKNOWN; ORIG1AP2021-01-14STANDARD

Submissions Property Types

ORIG1Null7

TE Codes

001PrescriptionAB

CDER Filings

VISTAPHARM
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 213951
            [companyName] => VISTAPHARM
            [docInserts] => ["",""]
            [products] => [{"drugName":"ACYCLOVIR","activeIngredients":"ACYCLOVIR","strength":"200MG\/5ML","dosageForm":"SUSPENSION;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"01\/14\/2021","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2021-01-14
        )

)

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