ABBOTT FDA Approval ANDA 089362

ANDA 089362

ABBOTT

FDA Drug Application

Application #089362

Application Sponsors

ANDA 089362ABBOTT

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION20%0LIDOCAINE HYDROCHLORIDELIDOCAINE HYDROCHLORIDE

FDA Submissions

ORIG1AP1988-05-25

CDER Filings

ABBOTT
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 89362
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"LIDOCAINE HYDROCHLORIDE","activeIngredients":"LIDOCAINE HYDROCHLORIDE","strength":"20%","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"LIDOCAINE HYDROCHLORIDE","submission":"LIDOCAINE HYDROCHLORIDE","actionType":"20%","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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