UCB INC FDA Approval ANDA 073121

ANDA 073121

UCB INC

FDA Drug Application

Application #073121

Application Sponsors

ANDA 073121UCB INC

Marketing Status

Discontinued001

Application Products

001TABLET;ORALEQ 4MG BASE0ALBUTEROL SULFATEALBUTEROL SULFATE

CDER Filings

UCB INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 73121
            [companyName] => UCB INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"ALBUTEROL SULFATE","activeIngredients":"ALBUTEROL SULFATE","strength":"EQ 4MG BASE","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"ALBUTEROL SULFATE","submission":"ALBUTEROL SULFATE","actionType":"EQ 4MG BASE","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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