SUN PHARM INDS INC FDA Approval ANDA 040899

ANDA 040899

SUN PHARM INDS INC

FDA Drug Application

Application #040899

Application Sponsors

ANDA 040899SUN PHARM INDS INC

Marketing Status

Discontinued001
Discontinued002
Discontinued003

Application Products

001TABLET;ORAL10MG0HYDROXYZINE HYDROCHLORIDEHYDROXYZINE HYDROCHLORIDE
002TABLET;ORAL25MG0HYDROXYZINE HYDROCHLORIDEHYDROXYZINE HYDROCHLORIDE
003TABLET;ORAL50MG0HYDROXYZINE HYDROCHLORIDEHYDROXYZINE HYDROCHLORIDE

FDA Submissions

ORIG1AP2008-06-10
LABELING; LabelingSUPPL3AP2014-06-03STANDARD
LABELING; LabelingSUPPL4AP2016-03-30STANDARD
LABELING; LabelingSUPPL5AP2016-11-08STANDARD

Submissions Property Types

ORIG1Null1
SUPPL3Null7
SUPPL4Null7
SUPPL5Null15

CDER Filings

SUN PHARM INDS INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 40899
            [companyName] => SUN PHARM INDS INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"HYDROXYZINE HYDROCHLORIDE","activeIngredients":"HYDROXYZINE HYDROCHLORIDE","strength":"10MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"HYDROXYZINE HYDROCHLORIDE","activeIngredients":"HYDROXYZINE HYDROCHLORIDE","strength":"25MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"HYDROXYZINE HYDROCHLORIDE","activeIngredients":"HYDROXYZINE HYDROCHLORIDE","strength":"50MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"HYDROXYZINE HYDROCHLORIDE","submission":"HYDROXYZINE HYDROCHLORIDE","actionType":"10MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"HYDROXYZINE HYDROCHLORIDE","submission":"HYDROXYZINE HYDROCHLORIDE","actionType":"25MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"HYDROXYZINE HYDROCHLORIDE","submission":"HYDROXYZINE HYDROCHLORIDE","actionType":"50MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.