CHARTWELL RX FDA Approval ANDA 085952

ANDA 085952

CHARTWELL RX

FDA Drug Application

Application #085952

Application Sponsors

ANDA 085952CHARTWELL RX

Marketing Status

Discontinued001

Application Products

001ELIXIR;ORAL80MG/15ML0THEOPHYLLINETHEOPHYLLINE

CDER Filings

CHARTWELL RX
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 85952
            [companyName] => CHARTWELL RX
            [docInserts] => ["",""]
            [products] => [{"drugName":"THEOPHYLLINE","activeIngredients":"THEOPHYLLINE","strength":"80MG\/15ML","dosageForm":"ELIXIR;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"THEOPHYLLINE","submission":"THEOPHYLLINE","actionType":"80MG\/15ML","submissionClassification":"ELIXIR;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.