ANDA 071274

EUROHLTH INTL SARL

FDA Drug Application

Application #071274

Application Sponsors

ANDA 071274

EUROHLTH INTL SARL

Marketing Status

• Discontinued: 001

Application Products

001

INJECTABLE;INJECTION

1MG/ML

0

NALOXONE HYDROCHLORIDE

NALOXONE HYDROCHLORIDE

FDA Submissions

ORIG

1

AP

1988-05-24

CDER Filings

EUROHLTH INTL SARL

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 71274
            [companyName] => EUROHLTH INTL SARL
            [docInserts] => ["",""]
            [products] => [{"drugName":"NALOXONE HYDROCHLORIDE","activeIngredients":"NALOXONE HYDROCHLORIDE","strength":"1MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"NALOXONE HYDROCHLORIDE","submission":"NALOXONE HYDROCHLORIDE","actionType":"1MG\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)