ANDA 077173

SUN PHARM INDS LTD

FDA Drug Application

Application #077173

Application Sponsors

ANDA 077173

SUN PHARM INDS LTD

Marketing Status

• Discontinued: 001

Application Products

001

INJECTABLE;INJECTION

EQ 2MG BASE/ML

0

ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE

ONDANSETRON HYDROCHLORIDE

FDA Submissions

	ORIG	1	AP	2006-12-26
LABELING; Labeling	SUPPL	3	AP	2015-07-02	STANDARD
LABELING; Labeling	SUPPL	5	AP	2015-07-02	STANDARD

Submissions Property Types

SUPPL	3	Null	7
SUPPL	5	Null	7

CDER Filings

SUN PHARM INDS LTD

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 77173
            [companyName] => SUN PHARM INDS LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE","activeIngredients":"ONDANSETRON HYDROCHLORIDE","strength":"EQ 2MG BASE\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE","submission":"ONDANSETRON HYDROCHLORIDE","actionType":"EQ 2MG BASE\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)