ANDA 207692

AKORN

FDA Drug Application

Application #207692

Application Sponsors

ANDA 207692

AKORN

Marketing Status

• Prescription: 001

Application Products

001

SOLUTION;INTRAVENOUS

0.005MG/ML (0.005MG/ML)

0

PARICALCITOL

PARICALCITOL

FDA Submissions

UNKNOWN;

ORIG

1

AP

2017-10-16

STANDARD

Submissions Property Types

ORIG

1

Null

15

TE Codes

001

Prescription

AP

CDER Filings

AKORN

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 207692
            [companyName] => AKORN
            [docInserts] => ["",""]
            [products] => [{"drugName":"PARICALCITOL","activeIngredients":"PARICALCITOL","strength":"0.005MG\/ML (0.005MG\/ML)","dosageForm":"SOLUTION;INTRAVENOUS","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"10\/16\/2017","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2017-10-16
        )

)