3M FDA Approval NDA 012126

NDA 012126

3M

FDA Drug Application

Application #012126

Application Sponsors

NDA 0121263M

Marketing Status

Discontinued001

Application Products

001SYRUP;ORAL25MG/5ML0ULOCHLOPHEDIANOL HYDROCHLORIDE

CDER Filings

3M
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 12126
            [companyName] => 3M
            [docInserts] => ["",""]
            [products] => [{"drugName":"ULO","activeIngredients":"CHLOPHEDIANOL HYDROCHLORIDE","strength":"25MG\/5ML","dosageForm":"SYRUP;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"ULO","submission":"CHLOPHEDIANOL HYDROCHLORIDE","actionType":"25MG\/5ML","submissionClassification":"SYRUP;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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