CAREFUSION 2200 FDA Approval NDA 019793

NDA 019793

CAREFUSION 2200

FDA Drug Application

Application #019793

Application Sponsors

NDA 019793CAREFUSION 2200

Marketing Status

Discontinued001

Application Products

001SPONGE;TOPICAL4%0PHARMASEAL SCRUB CARECHLORHEXIDINE GLUCONATE

FDA Submissions

TYPE 5; Type 5 - New Formulation or New ManufacturerORIG1AP1988-12-02STANDARD
MANUF (CMC); Manufacturing (CMC)SUPPL2AP1999-01-26STANDARD
MANUF (CMC); Manufacturing (CMC)SUPPL5AP2015-08-14STANDARD

Submissions Property Types

SUPPL1Null0
SUPPL2Null0
SUPPL5Null0

CDER Filings

CAREFUSION 2200
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 19793
            [companyName] => CAREFUSION 2200
            [docInserts] => ["",""]
            [products] => [{"drugName":"PHARMASEAL SCRUB CARE","activeIngredients":"CHLORHEXIDINE GLUCONATE","strength":"4%","dosageForm":"SPONGE;TOPICAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"PHARMASEAL SCRUB CARE","submission":"CHLORHEXIDINE GLUCONATE","actionType":"4%","submissionClassification":"SPONGE;TOPICAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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