NAVINTA LLC FDA Approval ANDA 202938

ANDA 202938

NAVINTA LLC

FDA Drug Application

Application #202938

Application Sponsors

ANDA 202938NAVINTA LLC

Marketing Status

Prescription001

Application Products

001INJECTABLE;INJECTION20MG/ML0HYDRALAZINE HYDROCHLORIDEHYDRALAZINE HYDROCHLORIDE

FDA Submissions

UNKNOWN; ORIG1AP2013-03-28

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAP

CDER Filings

NAVINTA LLC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 202938
            [companyName] => NAVINTA LLC
            [docInserts] => ["",""]
            [products] => [{"drugName":"HYDRALAZINE HYDROCHLORIDE","activeIngredients":"HYDRALAZINE HYDROCHLORIDE","strength":"20MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"03\/28\/2013","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2013-03-28
        )

)

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