WATSON LABS TEVA FDA Approval ANDA 078984

ANDA 078984

WATSON LABS TEVA

FDA Drug Application

Application #078984

Documents

Letter2010-06-30

Application Sponsors

ANDA 078984WATSON LABS TEVA

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL1MG0ANASTROZOLEANASTROZOLE

FDA Submissions

ORIG1AP2010-06-28

Submissions Property Types

ORIG1Null7

CDER Filings

WATSON LABS TEVA
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 78984
            [companyName] => WATSON LABS TEVA
            [docInserts] => ["",""]
            [products] => [{"drugName":"ANASTROZOLE","activeIngredients":"ANASTROZOLE","strength":"1MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"ANASTROZOLE","submission":"ANASTROZOLE","actionType":"1MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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