FUTURE PAK FDA Approval ANDA 070998

ANDA 070998

FUTURE PAK

FDA Drug Application

Application #070998

Application Sponsors

ANDA 070998FUTURE PAK

Marketing Status

Discontinued001

Application Products

001TABLET, EXTENDED RELEASE;ORAL8MEQ0K+8POTASSIUM CHLORIDE

FDA Submissions

ORIG1AP1993-01-25
MANUF (CMC); Manufacturing (CMC)SUPPL6AP1995-06-23
MANUF (CMC); Manufacturing (CMC)SUPPL9AP1995-06-23

Submissions Property Types

SUPPL6Null0
SUPPL9Null0

CDER Filings

FUTURE PAK
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70998
            [companyName] => FUTURE PAK
            [docInserts] => ["",""]
            [products] => [{"drugName":"K+8","activeIngredients":"POTASSIUM CHLORIDE","strength":"8MEQ","dosageForm":"TABLET, EXTENDED RELEASE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"K+8","submission":"POTASSIUM CHLORIDE","actionType":"8MEQ","submissionClassification":"TABLET, EXTENDED RELEASE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 2020-11-06
        )

)

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