NDA 020784

SANOFI AVENTIS US

FDA Drug Application

Application #020784

Documents

• Letter: 2004-04-20
• Review: 2007-07-03

Application Sponsors

NDA 020784

SANOFI AVENTIS US

Marketing Status

• Discontinued: 001

Application Products

001

SPRAY, METERED;NASAL

0.055MG/SPRAY

0

NASACORT HFA

TRIAMCINOLONE ACETONIDE

FDA Submissions

TYPE 3; Type 3 - New Dosage Form

ORIG

1

AP

2004-04-07

STANDARD

CDER Filings

SANOFI AVENTIS US

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 20784
            [companyName] => SANOFI AVENTIS US
            [docInserts] => ["",""]
            [products] => [{"drugName":"NASACORT HFA","activeIngredients":"TRIAMCINOLONE ACETONIDE","strength":"0.055MG\/SPRAY","dosageForm":"SPRAY, METERED;NASAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"NASACORT HFA","submission":"TRIAMCINOLONE ACETONIDE","actionType":"0.055MG\/SPRAY","submissionClassification":"SPRAY, METERED;NASAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)