SUN PHARM FDA Approval ANDA 203650

ANDA 203650

SUN PHARM

FDA Drug Application

Application #203650

Application Sponsors

ANDA 203650SUN PHARM

Marketing Status

Prescription001

Application Products

001TABLET, EXTENDED RELEASE;ORAL300MG0BUPROPION HYDROCHLORIDEBUPROPION HYDROCHLORIDE

FDA Submissions

UNKNOWN; ORIG1AP2020-12-31

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAB3

CDER Filings

SUN PHARM
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 203650
            [companyName] => SUN PHARM
            [docInserts] => ["",""]
            [products] => [{"drugName":"BUPROPION HYDROCHLORIDE","activeIngredients":"BUPROPION HYDROCHLORIDE","strength":"300MG","dosageForm":"TABLET, EXTENDED RELEASE;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"12\/31\/2020","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2020-12-31
        )

)

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