NESHER PHARMS FDA Approval ANDA 076044

ANDA 076044

NESHER PHARMS

FDA Drug Application

Application #076044

Documents

Letter2003-04-10

Application Sponsors

ANDA 076044NESHER PHARMS

Marketing Status

Discontinued001

Application Products

001TABLET, EXTENDED RELEASE;ORAL20MEQ0POTASSIUM CHLORIDEPOTASSIUM CHLORIDE

FDA Submissions

ORIG1AP2002-04-05
LABELING; LabelingSUPPL2AP2002-10-02

Submissions Property Types

ORIG1Null0
SUPPL2Null0

CDER Filings

NESHER PHARMS
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 76044
            [companyName] => NESHER PHARMS
            [docInserts] => ["",""]
            [products] => [{"drugName":"POTASSIUM CHLORIDE","activeIngredients":"POTASSIUM CHLORIDE","strength":"20MEQ","dosageForm":"TABLET, EXTENDED RELEASE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"POTASSIUM CHLORIDE","submission":"POTASSIUM CHLORIDE","actionType":"20MEQ","submissionClassification":"TABLET, EXTENDED RELEASE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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