BASF FDA Approval ANDA 070083

ANDA 070083

BASF

FDA Drug Application

Application #070083

Application Sponsors

ANDA 070083BASF

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL400MG0IBUIBUPROFEN

FDA Submissions

ORIG1AP1985-02-22
MANUF (CMC); Manufacturing (CMC)SUPPL2AP1986-01-16
MANUF (CMC); Manufacturing (CMC)SUPPL3AP1986-01-16
MANUF (CMC); Manufacturing (CMC)SUPPL4AP1986-01-16
MANUF (CMC); Manufacturing (CMC)SUPPL5AP1986-01-16
MANUF (CMC); Manufacturing (CMC)SUPPL6AP1986-05-23
LABELING; LabelingSUPPL8AP1988-03-01
MANUF (CMC); Manufacturing (CMC)SUPPL9AP1989-02-14
LABELING; LabelingSUPPL10AP1989-02-14
LABELING; LabelingSUPPL12AP1989-09-06
LABELING; LabelingSUPPL13AP1991-08-06
LABELING; LabelingSUPPL14AP1991-10-24
LABELING; LabelingSUPPL15AP1992-03-11
LABELING; LabelingSUPPL16AP1993-05-03
MANUF (CMC); Manufacturing (CMC)SUPPL17AP1994-09-30
MANUF (CMC); Manufacturing (CMC)SUPPL18AP1994-09-30
MANUF (CMC); Manufacturing (CMC)SUPPL19AP1995-08-11
LABELING; LabelingSUPPL20AP1995-02-15

Submissions Property Types

ORIG1Null0
SUPPL2Null0
SUPPL3Null0
SUPPL4Null0
SUPPL5Null0
SUPPL6Null0
SUPPL8Null0
SUPPL9Null0
SUPPL10Null0
SUPPL12Null0
SUPPL13Null0
SUPPL14Null0
SUPPL15Null0
SUPPL16Null0
SUPPL17Null0
SUPPL18Null0
SUPPL19Null0
SUPPL20Null0

CDER Filings

BASF
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70083
            [companyName] => BASF
            [docInserts] => ["",""]
            [products] => [{"drugName":"IBU","activeIngredients":"IBUPROFEN","strength":"400MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"IBU","submission":"IBUPROFEN","actionType":"400MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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