LANNETT CO INC FDA Approval ANDA 078496

ANDA 078496

LANNETT CO INC

FDA Drug Application

Application #078496

Application Sponsors

ANDA 078496LANNETT CO INC

Marketing Status

Discontinued001

Application Products

001SYRUP;ORAL5MG/5ML0CETIRIZINE HYDROCHLORIDECETIRIZINE HYDROCHLORIDE

FDA Submissions

UNKNOWN; ORIG1AP2009-09-25
LABELING; LabelingSUPPL5AP2016-11-08STANDARD
LABELING; LabelingSUPPL6AP2020-02-14STANDARD

Submissions Property Types

ORIG1Null7
SUPPL5Null15
SUPPL6Null15

CDER Filings

LANNETT CO INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 78496
            [companyName] => LANNETT CO INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"CETIRIZINE HYDROCHLORIDE","activeIngredients":"CETIRIZINE HYDROCHLORIDE","strength":"5MG\/5ML","dosageForm":"SYRUP;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"CETIRIZINE HYDROCHLORIDE","submission":"CETIRIZINE HYDROCHLORIDE","actionType":"5MG\/5ML","submissionClassification":"SYRUP;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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