ABBOTT FDA Approval ANDA 086333

ANDA 086333

ABBOTT

FDA Drug Application

Application #086333

Application Sponsors

ANDA 086333ABBOTT

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL500MG;5MG0VICOPRINASPIRIN; HYDROCODONE BITARTRATE

FDA Submissions

MANUF (CMC); Manufacturing (CMC)SUPPL1AP1983-12-14

Submissions Property Types

SUPPL1Null0

CDER Filings

ABBOTT
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 86333
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"VICOPRIN","activeIngredients":"ASPIRIN; HYDROCODONE BITARTRATE","strength":"500MG;5MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"VICOPRIN","submission":"ASPIRIN; HYDROCODONE BITARTRATE","actionType":"500MG;5MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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