HONG KONG FDA Approval ANDA 213461

ANDA 213461

HONG KONG

FDA Drug Application

Application #213461

Application Sponsors

ANDA 213461HONG KONG

Marketing Status

Prescription001

Application Products

001SOLUTION;INTRAVENOUS20MG/20ML (1MG/ML)0CLOFARABINECLOFARABINE

FDA Submissions

UNKNOWN; ORIG1AP2020-10-23STANDARD

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAP

CDER Filings

HONG KONG
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 213461
            [companyName] => HONG KONG
            [docInserts] => ["",""]
            [products] => [{"drugName":"CLOFARABINE","activeIngredients":"CLOFARABINE","strength":"20MG\/20ML (1MG\/ML)","dosageForm":"SOLUTION;INTRAVENOUS","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"CLOFARABINE","submission":"CLOFARABINE","actionType":"20MG\/20ML (1MG\/ML)","submissionClassification":"SOLUTION;INTRAVENOUS","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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