ANDA 040065

BAUSCH AND LOMB

FDA Drug Application

Application #040065

Application Sponsors

ANDA 040065

BAUSCH AND LOMB

Marketing Status

• Discontinued: 001

Application Products

001

SOLUTION/DROPS;OPHTHALMIC

EQ 0.11% PHOSPHATE

0

PREDNISOLONE SODIUM PHOSPHATE

PREDNISOLONE SODIUM PHOSPHATE

FDA Submissions

	ORIG	1	AP	1994-07-29
MANUF (CMC); Manufacturing (CMC)	SUPPL	2	AP	1999-06-07
MANUF (CMC); Manufacturing (CMC)	SUPPL	3	AP	2000-05-18
MANUF (CMC); Manufacturing (CMC)	SUPPL	4	AP	2000-04-28
MANUF (CMC); Manufacturing (CMC)	SUPPL	6	AP	2000-06-27
MANUF (CMC); Manufacturing (CMC)	SUPPL	7	AP	2000-10-05
MANUF (CMC); Manufacturing (CMC)	SUPPL	8	AP	2001-03-07
MANUF (CMC); Manufacturing (CMC)	SUPPL	10	AP	2001-11-27

Submissions Property Types

SUPPL	2	Null	0
SUPPL	3	Null	0
SUPPL	4	Null	0
SUPPL	6	Null	0
SUPPL	7	Null	0
SUPPL	8	Null	0
SUPPL	10	Null	0

CDER Filings

BAUSCH AND LOMB

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 40065
            [companyName] => BAUSCH AND LOMB
            [docInserts] => ["",""]
            [products] => [{"drugName":"PREDNISOLONE SODIUM PHOSPHATE","activeIngredients":"PREDNISOLONE SODIUM PHOSPHATE","strength":"EQ 0.11% PHOSPHATE","dosageForm":"SOLUTION\/DROPS;OPHTHALMIC","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"PREDNISOLONE SODIUM PHOSPHATE","submission":"PREDNISOLONE SODIUM PHOSPHATE","actionType":"EQ 0.11% PHOSPHATE","submissionClassification":"SOLUTION\/DROPS;OPHTHALMIC","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)