EMCURE PHARMS LTD FDA Approval ANDA 206408

ANDA 206408

EMCURE PHARMS LTD

FDA Drug Application

Application #206408

Application Sponsors

ANDA 206408EMCURE PHARMS LTD

Marketing Status

Prescription001

Application Products

001INJECTABLE;INJECTION10MG/ML0PROPOFOLPROPOFOL

FDA Submissions

UNKNOWN; ORIG1AP2021-10-12STANDARD

Submissions Property Types

ORIG1Null7

TE Codes

001PrescriptionAB

CDER Filings

EMCURE PHARMS LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 206408
            [companyName] => EMCURE PHARMS LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"PROPOFOL","activeIngredients":"PROPOFOL","strength":"10MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"10\/12\/2021","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2021-10-12
        )

)

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