SUN PHARM INDS INC FDA Approval ANDA 091027

ANDA 091027

SUN PHARM INDS INC

FDA Drug Application

Application #091027

Application Sponsors

ANDA 091027SUN PHARM INDS INC

Marketing Status

Prescription001

Application Products

001TABLET;ORAL300MG0LITHIUM CARBONATELITHIUM CARBONATE

FDA Submissions

ORIG1AP2010-06-24

Submissions Property Types

ORIG1Null7

TE Codes

001PrescriptionAB

CDER Filings

SUN PHARM INDS INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 91027
            [companyName] => SUN PHARM INDS INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"LITHIUM CARBONATE","activeIngredients":"LITHIUM CARBONATE","strength":"300MG","dosageForm":"TABLET;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"LITHIUM CARBONATE","submission":"LITHIUM CARBONATE","actionType":"300MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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