LOTUS PHARM CO LTD FDA Approval ANDA 202684

ANDA 202684

LOTUS PHARM CO LTD

FDA Drug Application

Application #202684

Application Sponsors

ANDA 202684LOTUS PHARM CO LTD

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL0.75MG0LEVONORGESTRELLEVONORGESTREL

FDA Submissions

UNKNOWN; ORIG1AP2016-09-02

Submissions Property Types

ORIG1Null17

CDER Filings

LOTUS PHARM CO LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 202684
            [companyName] => LOTUS PHARM CO LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"LEVONORGESTREL","activeIngredients":"LEVONORGESTREL","strength":"0.75MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"09\/02\/2016","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2016-09-02
        )

)

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