ANDA 071002

BAYER

FDA Drug Application

Application #071002

Application Sponsors

ANDA 071002

BAYER

Marketing Status

• Discontinued: 001

Application Products

001

CAPSULE;ORAL

200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**

0

MIDOL

IBUPROFEN

CDER Filings

BAYER

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 71002
            [companyName] => BAYER
            [docInserts] => ["",""]
            [products] => [{"drugName":"MIDOL","activeIngredients":"IBUPROFEN","strength":"200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"MIDOL","submission":"IBUPROFEN","actionType":"200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**","submissionClassification":"CAPSULE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)