DR REDDYS LABS LTD FDA Approval ANDA 090930

ANDA 090930

DR REDDYS LABS LTD

FDA Drug Application

Application #090930

Application Sponsors

ANDA 090930DR REDDYS LABS LTD

Marketing Status

None (Tentative Approval)001

Application Products

001TABLET; ORAL85MG; 500MG0SUMATRIPTAN; NAPROXEN SODIUMSUMATRIPTAN; NAPROXEN SODIUM

FDA Submissions

ORIG1TA2011-01-20

CDER Filings

DR REDDYS LABS LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 90930
            [companyName] => DR REDDYS LABS LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"SUMATRIPTAN; NAPROXEN SODIUM","activeIngredients":"SUMATRIPTAN; NAPROXEN SODIUM","strength":"85MG; 500MG","dosageForm":"TABLET; ORAL","marketingStatus":"None (Tentative Approval)","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"SUMATRIPTAN; NAPROXEN SODIUM","submission":"SUMATRIPTAN; NAPROXEN SODIUM","actionType":"85MG; 500MG","submissionClassification":"TABLET; ORAL","reviewPriority":"None (Tentative Approval)","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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