AKORN INC FDA Approval ANDA 202585

ANDA 202585

AKORN INC

FDA Drug Application

Application #202585

Application Sponsors

ANDA 202585AKORN INC

Marketing Status

Prescription001

Application Products

001INJECTABLE;INJECTIONEQ 200MCG BASE/2ML (EQ 100MCG BASE/ML)0DEXMEDETOMIDINE HYDROCHLORIDEDEXMEDETOMIDINE HYDROCHLORIDE

FDA Submissions

UNKNOWN; ORIG1AP2014-11-24

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAP

CDER Filings

AKORN INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 202585
            [companyName] => AKORN INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"DEXMEDETOMIDINE HYDROCHLORIDE","activeIngredients":"DEXMEDETOMIDINE HYDROCHLORIDE","strength":"EQ 200MCG BASE\/2ML (EQ 100MCG BASE\/ML)","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"11\/24\/2014","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => [{"actionDate":"06\/19\/2020","submission":"SUPPL-1","supplementCategories":"Labeling-Package Insert","inserts":"[]","notes":"> Label is not available on this site."}]
            [actionDate] => 2020-06-19
        )

)

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.