ANDA 206710

LOTUS PHARM CO LTD

FDA Drug Application

Application #206710

Application Sponsors

ANDA 206710

LOTUS PHARM CO LTD

Marketing Status

• Discontinued: 001
• Discontinued: 002
• Discontinued: 003

Application Products

001	CAPSULE;ORAL	1MCG	0	PARICALCITOL	PARICALCITOL
002	CAPSULE;ORAL	2MCG	0	PARICALCITOL	PARICALCITOL
003	CAPSULE;ORAL	4MCG	0	PARICALCITOL	PARICALCITOL

FDA Submissions

UNKNOWN;

ORIG

1

AP

2016-02-24

STANDARD

Submissions Property Types

ORIG

1

Null

7

CDER Filings

LOTUS PHARM CO LTD

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 206710
            [companyName] => LOTUS PHARM CO LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"PARICALCITOL","activeIngredients":"PARICALCITOL","strength":"1MCG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"PARICALCITOL","activeIngredients":"PARICALCITOL","strength":"2MCG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"PARICALCITOL","activeIngredients":"PARICALCITOL","strength":"4MCG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"02\/24\/2016","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2016-02-24
        )

)