SANOFI AVENTIS US FDA Approval NDA 019498

NDA 019498

SANOFI AVENTIS US

FDA Drug Application

Application #019498

Application Sponsors

NDA 019498SANOFI AVENTIS US

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION200 UNITS/VIAL0PARATHARTERIPARATIDE ACETATE

CDER Filings

SANOFI AVENTIS US
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 19498
            [companyName] => SANOFI AVENTIS US
            [docInserts] => ["",""]
            [products] => [{"drugName":"PARATHAR","activeIngredients":"TERIPARATIDE ACETATE","strength":"200 UNITS\/VIAL","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"PARATHAR","submission":"TERIPARATIDE ACETATE","actionType":"200 UNITS\/VIAL","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.