HI TECH FDA Approval ANDA 208809

ANDA 208809

HI TECH

FDA Drug Application

Application #208809

Application Sponsors

ANDA 208809HI TECH

Marketing Status

Prescription001

Application Products

001SOLUTION;ORAL100MG/5ML0MORPHINE SULFATEMORPHINE SULFATE

FDA Submissions

UNKNOWN; ORIG1AP2017-07-06STANDARD
LABELING; LabelingSUPPL2AP2020-02-10STANDARD
LABELING; LabelingSUPPL5AP2020-02-10STANDARD

Submissions Property Types

ORIG1Null15
SUPPL2Null7
SUPPL5Null15

TE Codes

001PrescriptionAA

CDER Filings

AKORN
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 208809
            [companyName] => AKORN
            [docInserts] => ["",""]
            [products] => [{"drugName":"MORPHINE SULFATE","activeIngredients":"MORPHINE SULFATE","strength":"100MG\/5ML","dosageForm":"SOLUTION;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"07\/06\/2017","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => [{"actionDate":"02\/10\/2020","submission":"SUPPL-5","supplementCategories":"Labeling-Package Insert","inserts":"[]","notes":"> Label is not available on this site."},{"actionDate":"02\/10\/2020","submission":"SUPPL-2","supplementCategories":"Labeling-Package Insert","inserts":"[]","notes":"> Label is not available on this site."},{"actionDate":"09\/18\/2018","submission":"SUPPL-1","supplementCategories":"REMS - PROPOSAL - D-N-A","inserts":"[]","notes":"> Label is not available on this site."}]
            [actionDate] => 2020-02-10
        )

)

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