ANDA 071555

ABBOTT

FDA Drug Application

Application #071555

Application Sponsors

ANDA 071555

ABBOTT

Marketing Status

• Discontinued: 001

Application Products

001

INJECTABLE;INJECTION

50MG/VIAL

0

NITROPRESS

SODIUM NITROPRUSSIDE

FDA Submissions

	ORIG	1	AP	1987-11-16
LABELING; Labeling	SUPPL	2	AP	1990-12-07
LABELING; Labeling	SUPPL	3	AP	1992-02-03

CDER Filings

ABBOTT

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 71555
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"NITROPRESS","activeIngredients":"SODIUM NITROPRUSSIDE","strength":"50MG\/VIAL","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"NITROPRESS","submission":"SODIUM NITROPRUSSIDE","actionType":"50MG\/VIAL","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)