ANDA 075787

SUN PHARM INDUSTRIES

FDA Drug Application

Application #075787

Documents

• Other Important Information from FDA: 2005-08-01

Application Sponsors

ANDA 075787

SUN PHARM INDUSTRIES

Marketing Status

• Discontinued: 001
• Discontinued: 002

Application Products

001	CAPSULE;ORAL	EQ 10MG BASE	0	FLUOXETINE	FLUOXETINE HYDROCHLORIDE
002	CAPSULE;ORAL	EQ 20MG BASE	0	FLUOXETINE	FLUOXETINE HYDROCHLORIDE

FDA Submissions

	ORIG	1	AP	2002-01-29
LABELING; Labeling	SUPPL	4	AP	2005-06-30
LABELING; Labeling	SUPPL	11	AP	2007-06-29
LABELING; Labeling	SUPPL	12	AP	2007-06-29

CDER Filings

SUN PHARM INDUSTRIES

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 75787
            [companyName] => SUN PHARM INDUSTRIES
            [docInserts] => ["",""]
            [products] => [{"drugName":"FLUOXETINE","activeIngredients":"FLUOXETINE HYDROCHLORIDE","strength":"EQ 10MG BASE","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"FLUOXETINE","activeIngredients":"FLUOXETINE HYDROCHLORIDE","strength":"EQ 20MG BASE","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"FLUOXETINE","submission":"FLUOXETINE HYDROCHLORIDE","actionType":"EQ 10MG BASE","submissionClassification":"CAPSULE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"FLUOXETINE","submission":"FLUOXETINE HYDROCHLORIDE","actionType":"EQ 20MG BASE","submissionClassification":"CAPSULE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)