BECTON DICKINSON FDA Approval NDA 017452

NDA 017452

BECTON DICKINSON

FDA Drug Application

Application #017452

Application Sponsors

NDA 017452BECTON DICKINSON

Marketing Status

Discontinued001

Application Products

001SPONGE;TOPICAL450MG0E-Z SCRUBHEXACHLOROPHENE

FDA Submissions

TYPE 3; Type 3 - New Dosage FormORIG1AP1976-07-08STANDARD
MANUF (CMC); Manufacturing (CMC)SUPPL2AP1985-08-21STANDARD
MANUF (CMC); Manufacturing (CMC)SUPPL3AP1988-11-09STANDARD

Submissions Property Types

SUPPL1Null0
SUPPL2Null0
SUPPL3Null0

CDER Filings

BECTON DICKINSON
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 17452
            [companyName] => BECTON DICKINSON
            [docInserts] => ["",""]
            [products] => [{"drugName":"E-Z SCRUB","activeIngredients":"HEXACHLOROPHENE","strength":"450MG","dosageForm":"SPONGE;TOPICAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"E-Z SCRUB","submission":"HEXACHLOROPHENE","actionType":"450MG","submissionClassification":"SPONGE;TOPICAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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