SMITH AND NEPHEW FDA Approval ANDA 070802

ANDA 070802

SMITH AND NEPHEW

FDA Drug Application

Application #070802

Application Sponsors

ANDA 070802SMITH AND NEPHEW

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTIONEQ 5MG BASE/ML0HALOPERIDOLHALOPERIDOL LACTATE

CDER Filings

SMITH AND NEPHEW
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70802
            [companyName] => SMITH AND NEPHEW
            [docInserts] => ["",""]
            [products] => [{"drugName":"HALOPERIDOL","activeIngredients":"HALOPERIDOL LACTATE","strength":"EQ 5MG BASE\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"HALOPERIDOL","submission":"HALOPERIDOL LACTATE","actionType":"EQ 5MG BASE\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.