ANDA 203298

LOTUS PHARM CO LTD

FDA Drug Application

Application #203298

Application Sponsors

ANDA 203298

LOTUS PHARM CO LTD

Marketing Status

• Discontinued: 001

Application Products

001

CAPSULE;ORAL

667MG

0

CALCIUM ACETATE

CALCIUM ACETATE

FDA Submissions

UNKNOWN;

ORIG

1

AP

2016-07-26

Submissions Property Types

ORIG

1

Null

15

CDER Filings

LOTUS PHARM CO LTD

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 203298
            [companyName] => LOTUS PHARM CO LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"CALCIUM ACETATE","activeIngredients":"CALCIUM ACETATE","strength":"667MG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"07\/26\/2016","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2016-07-26
        )

)