HIKMA FDA Approval ANDA 077838

ANDA 077838

HIKMA

FDA Drug Application

Application #077838

Application Sponsors

ANDA 077838HIKMA

Marketing Status

Prescription001

Application Products

001INJECTABLE;INJECTION3MG/ML;EQ 3MG BASE/ML0BETAMETHASONE ACETATE AND BETAMETHASONE SODIUM PHOSPHATEBETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE

FDA Submissions

ORIG1AP2023-01-17

Submissions Property Types

ORIG1Null1

TE Codes

001PrescriptionAB

CDER Filings

HIKMA
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 77838
            [companyName] => HIKMA
            [docInserts] => ["",""]
            [products] => [{"drugName":"BETAMETHASONE ACETATE AND BETAMETHASONE SODIUM PHOSPHATE","activeIngredients":"BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE","strength":"3MG\/ML;EQ 3MG BASE\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"BETAMETHASONE ACETATE AND BETAMETHASONE SODIUM PHOSPHATE","submission":"BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE","actionType":"3MG\/ML;EQ 3MG BASE\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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