SUN PHARM INDS LTD FDA Approval ANDA 065207

ANDA 065207

SUN PHARM INDS LTD

FDA Drug Application

Application #065207

Application Sponsors

ANDA 065207SUN PHARM INDS LTD

Marketing Status

Discontinued002

Application Products

002FOR SUSPENSION;ORAL600MG/5ML;EQ 42.9MG BASE/5ML0AMOXICILLIN AND CLAVULANATE POTASSIUMAMOXICILLIN; CLAVULANATE POTASSIUM

FDA Submissions

ORIG1AP2007-01-30

CDER Filings

SUN PHARM INDS LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 65207
            [companyName] => SUN PHARM INDS LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"AMOXICILLIN AND CLAVULANATE POTASSIUM","activeIngredients":"AMOXICILLIN; CLAVULANATE POTASSIUM","strength":"600MG\/5ML;EQ 42.9MG BASE\/5ML","dosageForm":"FOR SUSPENSION;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"AMOXICILLIN AND CLAVULANATE POTASSIUM","submission":"AMOXICILLIN; CLAVULANATE POTASSIUM","actionType":"600MG\/5ML;EQ 42.9MG BASE\/5ML","submissionClassification":"FOR SUSPENSION;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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