ANDA 084081

SUN PHARM INDUSTRIES

FDA Drug Application

Application #084081

Application Sponsors

ANDA 084081

SUN PHARM INDUSTRIES

Marketing Status

• Discontinued: 001

Application Products

001

TABLET;ORAL

0.75MG

0

DEXAMETHASONE

DEXAMETHASONE

FDA Submissions

	ORIG	1	AP	1974-07-03
MANUF (CMC); Manufacturing (CMC)	SUPPL	35	AP	1982-03-11
MANUF (CMC); Manufacturing (CMC)	SUPPL	38	AP	1987-03-20
LABELING; Labeling	SUPPL	40	AP	1990-04-05
LABELING; Labeling	SUPPL	41	AP	1991-01-16
LABELING; Labeling	SUPPL	42	AP	1992-05-08
MANUF (CMC); Manufacturing (CMC)	SUPPL	43	AP	1992-04-03
MANUF (CMC); Manufacturing (CMC)	SUPPL	45	AP	1992-04-03
MANUF (CMC); Manufacturing (CMC)	SUPPL	46	AP	1994-10-11
MANUF (CMC); Manufacturing (CMC)	SUPPL	47	AP	1994-12-23
MANUF (CMC); Manufacturing (CMC)	SUPPL	48	AP	1998-12-01

Submissions Property Types

SUPPL	35	Null	0
SUPPL	38	Null	0
SUPPL	43	Null	0
SUPPL	45	Null	0
SUPPL	46	Null	0
SUPPL	47	Null	0
SUPPL	48	Null	0

CDER Filings

SUN PHARM INDUSTRIES

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 84081
            [companyName] => SUN PHARM INDUSTRIES
            [docInserts] => ["",""]
            [products] => [{"drugName":"DEXAMETHASONE","activeIngredients":"DEXAMETHASONE","strength":"0.75MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"DEXAMETHASONE","submission":"DEXAMETHASONE","actionType":"0.75MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)