NDA 016998

PARKE DAVIS

FDA Drug Application

Application #016998

Application Sponsors

NDA 016998

PARKE DAVIS

Marketing Status

• Discontinued: 002

Application Products

002

CREAM;TOPICAL

0.025%

0

UTICORT

BETAMETHASONE BENZOATE

FDA Submissions

TYPE 3; Type 3 - New Dosage Form	ORIG	1	AP	1974-06-28	STANDARD
LABELING; Labeling	SUPPL	4	AP	1974-12-13
LABELING; Labeling	SUPPL	7	AP	1978-11-21
LABELING; Labeling	SUPPL	9	AP	1981-03-13

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 16998
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)