MANKIND PHARMA FDA Approval ANDA 215880

ANDA 215880

MANKIND PHARMA

FDA Drug Application

Application #215880

Application Sponsors

ANDA 215880MANKIND PHARMA

Marketing Status

Prescription001

Application Products

001TABLET, DELAYED RELEASE;ORALEQ 40MG BASE0PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUM

FDA Submissions

UNKNOWN; ORIG1AP2022-07-26STANDARD

Submissions Property Types

ORIG1Null7

TE Codes

001PrescriptionAB

CDER Filings

MANKIND PHARMA
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 215880
            [companyName] => MANKIND PHARMA
            [docInserts] => ["",""]
            [products] => [{"drugName":"PANTOPRAZOLE SODIUM","activeIngredients":"PANTOPRAZOLE SODIUM","strength":"EQ 40MG BASE","dosageForm":"TABLET, DELAYED RELEASE;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"07\/26\/2022","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2022-07-26
        )

)

© 2022 FDA.report
This site is not affiliated with or endorsed by the FDA.