ABBOTT FDA Approval ANDA 083154

ANDA 083154

ABBOTT

FDA Drug Application

Application #083154

Application Sponsors

ANDA 083154ABBOTT

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION0.01MG/ML;1%0LIDOCAINE HYDROCHLORIDE W/ EPINEPHRINEEPINEPHRINE; LIDOCAINE HYDROCHLORIDE

FDA Submissions

ORIG1AP1972-12-20

CDER Filings

ABBOTT
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 83154
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"LIDOCAINE HYDROCHLORIDE W\/ EPINEPHRINE","activeIngredients":"EPINEPHRINE; LIDOCAINE HYDROCHLORIDE","strength":"0.01MG\/ML;1%","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"LIDOCAINE HYDROCHLORIDE W\/ EPINEPHRINE","submission":"EPINEPHRINE; LIDOCAINE HYDROCHLORIDE","actionType":"0.01MG\/ML;1%","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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