ABBOTT FDA Approval ANDA 070656

ANDA 070656

ABBOTT

FDA Drug Application

Application #070656

Application Sponsors

ANDA 070656ABBOTT

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION40MG/ML0DOPAMINE HYDROCHLORIDEDOPAMINE HYDROCHLORIDE

CDER Filings

ABBOTT
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70656
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"DOPAMINE HYDROCHLORIDE","activeIngredients":"DOPAMINE HYDROCHLORIDE","strength":"40MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"DOPAMINE HYDROCHLORIDE","submission":"DOPAMINE HYDROCHLORIDE","actionType":"40MG\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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