APOTEX INC FDA Approval ANDA 091572

ANDA 091572

APOTEX INC

FDA Drug Application

Application #091572

Application Sponsors

ANDA 091572APOTEX INC

Marketing Status

Prescription001

Application Products

001SPRAY, METERED;NASAL0.665MG/SPRAY0OLOPATADINE HYDROCHLORIDEOLOPATADINE HYDROCHLORIDE

FDA Submissions

ORIG1AP2014-10-08

Submissions Property Types

ORIG1Null19

TE Codes

001PrescriptionAB

CDER Filings

APOTEX INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 91572
            [companyName] => APOTEX INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"OLOPATADINE HYDROCHLORIDE","activeIngredients":"OLOPATADINE HYDROCHLORIDE","strength":"0.665MG\/SPRAY","dosageForm":"SPRAY, METERED;NASAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"OLOPATADINE HYDROCHLORIDE","submission":"OLOPATADINE HYDROCHLORIDE","actionType":"0.665MG\/SPRAY","submissionClassification":"SPRAY, METERED;NASAL","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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