LANNETT CO INC FDA Approval ANDA 078876

ANDA 078876

LANNETT CO INC

FDA Drug Application

Application #078876

Application Sponsors

ANDA 078876LANNETT CO INC

Marketing Status

Prescription001

Application Products

001SYRUP;ORAL5MG/5ML0CETIRIZINE HYDROCHLORIDECETIRIZINE HYDROCHLORIDE

FDA Submissions

ORIG1AP2012-05-11
LABELING; LabelingSUPPL4AP2016-11-08STANDARD
LABELING; LabelingSUPPL5AP2020-03-03STANDARD

Submissions Property Types

ORIG1Null42
SUPPL4Null7
SUPPL5Null15

TE Codes

001PrescriptionAA

CDER Filings

LANNETT CO INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 78876
            [companyName] => LANNETT CO INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"CETIRIZINE HYDROCHLORIDE","activeIngredients":"CETIRIZINE HYDROCHLORIDE","strength":"5MG\/5ML","dosageForm":"SYRUP;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"CETIRIZINE HYDROCHLORIDE","submission":"CETIRIZINE HYDROCHLORIDE","actionType":"5MG\/5ML","submissionClassification":"SYRUP;ORAL","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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