ASTRAZENECA FDA Approval ANDA 072081

ANDA 072081

ASTRAZENECA

FDA Drug Application

Application #072081

Application Sponsors

ANDA 072081ASTRAZENECA

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION0.02MG/ML0NALOXONE HYDROCHLORIDENALOXONE HYDROCHLORIDE

CDER Filings

ASTRAZENECA
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 72081
            [companyName] => ASTRAZENECA
            [docInserts] => ["",""]
            [products] => [{"drugName":"NALOXONE HYDROCHLORIDE","activeIngredients":"NALOXONE HYDROCHLORIDE","strength":"0.02MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"NALOXONE HYDROCHLORIDE","submission":"NALOXONE HYDROCHLORIDE","actionType":"0.02MG\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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