SUN PHARM INDS INC FDA Approval ANDA 075844

ANDA 075844

SUN PHARM INDS INC

FDA Drug Application

Application #075844

Application Sponsors

ANDA 075844SUN PHARM INDS INC

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL600MG0OXAPROZINOXAPROZIN

FDA Submissions

ORIG1AP2002-01-03
LABELING; LabelingSUPPL6AP2003-03-21
LABELING; LabelingSUPPL8AP2006-02-07
LABELING; LabelingSUPPL9AP2006-06-08
LABELING; LabelingSUPPL10AP2007-06-19
LABELING; LabelingSUPPL11AP2007-08-09

Submissions Property Types

SUPPL1Null0

CDER Filings

SUN PHARM INDS INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 75844
            [companyName] => SUN PHARM INDS INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"OXAPROZIN","activeIngredients":"OXAPROZIN","strength":"600MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"OXAPROZIN","submission":"OXAPROZIN","actionType":"600MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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