YAOPHARMA CO LTD FDA Approval ANDA 071700

ANDA 071700

YAOPHARMA CO LTD

FDA Drug Application

Application #071700

Application Sponsors

ANDA 071700YAOPHARMA CO LTD

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL125MG0METHYLDOPAMETHYLDOPA

FDA Submissions

ORIG1AP1988-03-02
LABELING; LabelingSUPPL2AP1993-02-12
MANUF (CMC); Manufacturing (CMC)SUPPL3AP1995-03-27
LABELING; LabelingSUPPL4AP1996-06-05

Submissions Property Types

SUPPL3Null0

CDER Filings

YAOPHARMA CO LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 71700
            [companyName] => YAOPHARMA CO LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"METHYLDOPA","activeIngredients":"METHYLDOPA","strength":"125MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"METHYLDOPA","submission":"METHYLDOPA","actionType":"125MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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