ANDA 087384

ABBOTT

FDA Drug Application

Application #087384

Application Sponsors

ANDA 087384

ABBOTT

Marketing Status

• Discontinued: 001

Application Products

001

TABLET;ORAL

50MG

0

CHLORTHALIDONE

CHLORTHALIDONE

FDA Submissions

	ORIG	1	AP	1981-03-06
MANUF (CMC); Manufacturing (CMC)	SUPPL	4	AP	1983-08-19
MANUF (CMC); Manufacturing (CMC)	SUPPL	7	AP	1991-06-27

Submissions Property Types

ORIG	1	Null	0
SUPPL	4	Null	0
SUPPL	7	Null	0

CDER Filings

ABBOTT

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 87384
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"CHLORTHALIDONE","activeIngredients":"CHLORTHALIDONE","strength":"50MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"CHLORTHALIDONE","submission":"CHLORTHALIDONE","actionType":"50MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)