CHARTWELL RX FDA Approval ANDA 084542

ANDA 084542

CHARTWELL RX

FDA Drug Application

Application #084542

Application Sponsors

ANDA 084542CHARTWELL RX

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL5MG0PREDNISOLONEPREDNISOLONE

CDER Filings

CHARTWELL RX
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 84542
            [companyName] => CHARTWELL RX
            [docInserts] => ["",""]
            [products] => [{"drugName":"PREDNISOLONE","activeIngredients":"PREDNISOLONE","strength":"5MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"PREDNISOLONE","submission":"PREDNISOLONE","actionType":"5MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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