ABBOTT FDA Approval ANDA 087364

ANDA 087364

ABBOTT

FDA Drug Application

Application #087364

Application Sponsors

ANDA 087364ABBOTT

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL25MG0CHLORTHALIDONECHLORTHALIDONE

FDA Submissions

ORIG1AP1981-03-06
MANUF (CMC); Manufacturing (CMC)SUPPL2AP1983-08-19
MANUF (CMC); Manufacturing (CMC)SUPPL3AP1987-11-18
MANUF (CMC); Manufacturing (CMC)SUPPL5AP1991-06-27

Submissions Property Types

ORIG1Null0
SUPPL2Null0
SUPPL3Null0
SUPPL5Null0

CDER Filings

ABBOTT
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 87364
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"CHLORTHALIDONE","activeIngredients":"CHLORTHALIDONE","strength":"25MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"CHLORTHALIDONE","submission":"CHLORTHALIDONE","actionType":"25MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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