ANDA 203112

LUPIN LTD

FDA Drug Application

Application #203112

Application Sponsors

ANDA 203112

LUPIN LTD

Marketing Status

• Prescription: 001

Application Products

001

CAPSULE;ORAL

324MG

0

QUININE SULFATE

QUININE SULFATE

FDA Submissions

UNKNOWN;

ORIG

1

AP

2015-04-24

Submissions Property Types

ORIG

1

Null

7

TE Codes

001

Prescription

AB

CDER Filings

LUPIN LTD

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 203112
            [companyName] => LUPIN LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"QUININE SULFATE","activeIngredients":"QUININE SULFATE","strength":"324MG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"04\/24\/2015","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2015-04-24
        )

)