ABBOTT FDA Approval ANDA 080385

ANDA 080385

ABBOTT

FDA Drug Application

Application #080385

Application Sponsors

ANDA 080385ABBOTT

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION50MG/ML0MEPERIDINE HYDROCHLORIDEMEPERIDINE HYDROCHLORIDE

CDER Filings

ABBOTT
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 80385
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"MEPERIDINE HYDROCHLORIDE","activeIngredients":"MEPERIDINE HYDROCHLORIDE","strength":"50MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"MEPERIDINE HYDROCHLORIDE","submission":"MEPERIDINE HYDROCHLORIDE","actionType":"50MG\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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