BAYER FDA Approval ANDA 071001

ANDA 071001

BAYER

FDA Drug Application

Application #071001

Application Sponsors

ANDA 071001BAYER

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL200MG0MIDOLIBUPROFEN

CDER Filings

BAYER
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 71001
            [companyName] => BAYER
            [docInserts] => ["",""]
            [products] => [{"drugName":"MIDOL","activeIngredients":"IBUPROFEN","strength":"200MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"MIDOL","submission":"IBUPROFEN","actionType":"200MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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