ANDA 208335

HEC PHARM USA INC

FDA Drug Application

Application #208335

Documents

• Letter: 2018-06-05

Application Sponsors

ANDA 208335

HEC PHARM USA INC

Marketing Status

• None (Tentative Approval): 001

Application Products

001

TABLET;ORAL

5MG

0

LINAGLIPTIN

LINAGLIPTIN

FDA Submissions

UNKNOWN;

ORIG

1

TA

2018-05-25

STANDARD

Submissions Property Types

ORIG

1

Null

31

TE Codes

001

Prescription

AB

CDER Filings

HEC PHARM USA INC

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 208335
            [companyName] => HEC PHARM USA INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"LINAGLIPTIN","activeIngredients":"LINAGLIPTIN","strength":"5MG","dosageForm":"TABLET;ORAL","marketingStatus":"None (Tentative Approval)","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"05\/25\/2018","submission":"ORIG-1","actionType":"Tentative Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[{\"name\":\"Letter (PDF)\",\"url\":\"https:\\\/\\\/www.accessdata.fda.gov\\\/drugsatfda_docs\\\/appletter\\\/2018\\\/208335Orig1s000ltr.pdf\"}]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2018-05-25
        )

)