ANCHEN PHARMS FDA Approval ANDA 078411

ANDA 078411

ANCHEN PHARMS

FDA Drug Application

Application #078411

Application Sponsors

ANDA 078411ANCHEN PHARMS

Marketing Status

Prescription001

Application Products

001TABLET, DELAYED RELEASE;ORALEQ 500MG VALPROIC ACID0DIVALPROEX SODIUMDIVALPROEX SODIUM

FDA Submissions

ORIG1AP2008-11-03

Submissions Property Types

SUPPL1Null8

TE Codes

001PrescriptionAB

CDER Filings

ANCHEN PHARMS
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 78411
            [companyName] => ANCHEN PHARMS
            [docInserts] => ["",""]
            [products] => [{"drugName":"DIVALPROEX SODIUM","activeIngredients":"DIVALPROEX SODIUM","strength":"EQ 500MG VALPROIC ACID","dosageForm":"TABLET, DELAYED RELEASE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"DIVALPROEX SODIUM","submission":"DIVALPROEX SODIUM","actionType":"EQ 500MG VALPROIC ACID","submissionClassification":"TABLET, DELAYED RELEASE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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