BAYER HEALTHCARE LLC FDA Approval NDA 018230

NDA 018230

BAYER HEALTHCARE LLC

FDA Drug Application

Application #018230

Application Sponsors

NDA 018230BAYER HEALTHCARE LLC

Marketing Status

Discontinued002

Application Products

002CREAM;VAGINAL1%0MYCELEX-7CLOTRIMAZOLE

FDA Submissions

TYPE 5; Type 5 - New Formulation or New ManufacturerORIG1AP1979-02-16STANDARD
LABELING; LabelingSUPPL2AP1980-09-08
LABELING; LabelingSUPPL3AP1980-10-23
LABELING; LabelingSUPPL5AP1982-01-27
MANUF (CMC); Manufacturing (CMC)SUPPL7AP1987-06-03STANDARD
LABELING; LabelingSUPPL8AP1990-06-14
EFFICACY; EfficacySUPPL9AP1991-12-26
MANUF (CMC); Manufacturing (CMC)SUPPL10AP1993-02-22STANDARD
LABELING; LabelingSUPPL11AP1992-10-08
LABELING; LabelingSUPPL13AP1995-02-13STANDARD
LABELING; LabelingSUPPL16AP1996-02-09STANDARD
MANUF (CMC); Manufacturing (CMC)SUPPL18AP1996-06-24STANDARD
MANUF (CMC); Manufacturing (CMC)SUPPL19AP1998-09-01STANDARD
MANUF (CMC); Manufacturing (CMC)SUPPL20AP2000-02-10STANDARD
MANUF (CMC); Manufacturing (CMC)SUPPL21AP2001-09-07STANDARD

Submissions Property Types

SUPPL1Null0
SUPPL7Null0
SUPPL10Null0
SUPPL18Null0
SUPPL19Null0
SUPPL20Null0
SUPPL21Null0

CDER Filings

BAYER HEALTHCARE LLC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 18230
            [companyName] => BAYER HEALTHCARE LLC
            [docInserts] => ["",""]
            [products] => [{"drugName":"MYCELEX-7","activeIngredients":"CLOTRIMAZOLE","strength":"1%","dosageForm":"CREAM;VAGINAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"MYCELEX-7","submission":"CLOTRIMAZOLE","actionType":"1%","submissionClassification":"CREAM;VAGINAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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