ANDA 210602

APTAPHARMA INC

FDA Drug Application

Application #210602

Application Sponsors

ANDA 210602

APTAPHARMA INC

Marketing Status

• Over-the-counter: 001

Application Products

001

SUSPENSION;ORAL

100MG/5ML

0

IBUPROFEN

IBUPROFEN

FDA Submissions

UNKNOWN;

ORIG

1

AP

2018-11-23

STANDARD

Submissions Property Types

ORIG

1

Null

7

CDER Filings

APTAPHARMA INC

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 210602
            [companyName] => APTAPHARMA INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"IBUPROFEN","activeIngredients":"IBUPROFEN","strength":"100MG\/5ML","dosageForm":"SUSPENSION;ORAL","marketingStatus":"Over-the-counter","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"11\/23\/2018","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2018-11-23
        )

)