ANDA 210467

SUN PHARM

FDA Drug Application

Application #210467

Application Sponsors

ANDA 210467

SUN PHARM

Marketing Status

• Discontinued: 001

Application Products

001

INJECTABLE;INJECTION

25MG/ML

0

SODIUM NITROPRUSSIDE

SODIUM NITROPRUSSIDE

FDA Submissions

UNKNOWN;

ORIG

1

AP

2018-11-26

STANDARD

Submissions Property Types

ORIG

1

Null

15

CDER Filings

SUN PHARM

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 210467
            [companyName] => SUN PHARM
            [docInserts] => ["",""]
            [products] => [{"drugName":"SODIUM NITROPRUSSIDE","activeIngredients":"SODIUM NITROPRUSSIDE","strength":"25MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"11\/26\/2018","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2018-11-26
        )

)