ANDA 063265

ABBOTT

FDA Drug Application

Application #063265

Application Sponsors

ANDA 063265

ABBOTT

Marketing Status

• Discontinued: 001

Application Products

001

INJECTABLE;INJECTION

EQ 250MG BASE/ML

0

AMIKACIN SULFATE

AMIKACIN SULFATE

FDA Submissions

ORIG

1

AP

1994-11-30

CDER Filings

ABBOTT

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 63265
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"AMIKACIN SULFATE","activeIngredients":"AMIKACIN SULFATE","strength":"EQ 250MG BASE\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"AMIKACIN SULFATE","submission":"AMIKACIN SULFATE","actionType":"EQ 250MG BASE\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)