NANJING KING-FRIEND FDA Approval ANDA 215860

ANDA 215860

NANJING KING-FRIEND

FDA Drug Application

Application #215860

Application Sponsors

ANDA 215860NANJING KING-FRIEND

Marketing Status

Prescription001

Application Products

001INJECTABLE;INTRAVENOUSEQ 40MG BASE/VIAL0PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUM

FDA Submissions

UNKNOWN; ORIG1AP2022-08-29STANDARD

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAP

CDER Filings

NANJING KING-FRIEND
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 215860
            [companyName] => NANJING KING-FRIEND
            [docInserts] => ["",""]
            [products] => [{"drugName":"PANTOPRAZOLE SODIUM","activeIngredients":"PANTOPRAZOLE SODIUM","strength":"EQ 40MG BASE\/VIAL","dosageForm":"INJECTABLE;INTRAVENOUS","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"08\/29\/2022","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2022-08-29
        )

)

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