ANDA 206295

SUNSHINE LAKE

FDA Drug Application

Application #206295

Application Sponsors

ANDA 206295

SUNSHINE LAKE

Marketing Status

• Discontinued: 001

Application Products

001

TABLET;ORAL

EQ 400MG BASE

0

MOXIFLOXACIN HYDROCHLORIDE

MOXIFLOXACIN HYDROCHLORIDE

FDA Submissions

UNKNOWN;

ORIG

1

AP

2018-09-28

STANDARD

Submissions Property Types

ORIG

1

Null

15

CDER Filings

SUNSHINE

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 206295
            [companyName] => SUNSHINE
            [docInserts] => ["",""]
            [products] => [{"drugName":"MOXIFLOXACIN HYDROCHLORIDE","activeIngredients":"MOXIFLOXACIN HYDROCHLORIDE","strength":"EQ 400MG BASE","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"09\/28\/2018","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2018-09-28
        )

)