APOTEX CORP FDA Approval ANDA 211607

ANDA 211607

APOTEX CORP

FDA Drug Application

Application #211607

Documents

Letter2020-03-17

Application Sponsors

ANDA 211607APOTEX CORP

Marketing Status

None (Tentative Approval)001

Application Products

001CAPSULE;ORAL20MG0TASIMELTEONTASIMELTEON

FDA Submissions

UNKNOWN; ORIG1TA2020-02-03STANDARD

Submissions Property Types

ORIG1Null31

TE Codes

001PrescriptionAB

CDER Filings

APOTEX CORP
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 211607
            [companyName] => APOTEX CORP
            [docInserts] => ["",""]
            [products] => [{"drugName":"TASIMELTEON","activeIngredients":"TASIMELTEON","strength":"UNKNOWN","dosageForm":"UNKNOWN","marketingStatus":"None (Tentative Approval)","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"02\/03\/2020","submission":"ORIG-1","actionType":"Tentative Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[{\"name\":\"Letter (PDF)\",\"url\":\"https:\\\/\\\/www.accessdata.fda.gov\\\/drugsatfda_docs\\\/appletter\\\/2020\\\/211607Orig1s000TAltr.pdf\"}]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2020-02-03
        )

)

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