MORTON GROVE FDA Approval ANDA 089661

ANDA 089661

MORTON GROVE

FDA Drug Application

Application #089661

Application Sponsors

ANDA 089661MORTON GROVE

Marketing Status

Discontinued001

Application Products

001SOLUTION;ORAL50MG/5ML0HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE

CDER Filings

MORTON GROVE
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 89661
            [companyName] => MORTON GROVE
            [docInserts] => ["",""]
            [products] => [{"drugName":"HYDROCHLOROTHIAZIDE","activeIngredients":"HYDROCHLOROTHIAZIDE","strength":"50MG\/5ML","dosageForm":"SOLUTION;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"HYDROCHLOROTHIAZIDE","submission":"HYDROCHLOROTHIAZIDE","actionType":"50MG\/5ML","submissionClassification":"SOLUTION;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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