Drug History: PEDIAPRED

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9

Label and Approval History

Drug Name:	PEDIAPRED
FDA Application No:	(NDA) 019157
Active Ingredient(s):	PREDNISOLONE SODIUM PHOSPHATE
Company:	UCB INC

Label History

View the label approved on December 8, 2004 for PEDIAPRED, (NDA) 019157

To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
12/3/2004	018	Labeling Revision	Letter Label Review
1/3/2002	017	Manufacturing Change or Addition
1/21/1998	016	Labeling Revision	Review
12/17/1998	015	Patient Population Altered	Letter
5/29/1997	014	Control Supplement
12/17/1998	013	Labeling Revision	Letter
12/17/1998	012	Labeling Revision	Letter
12/17/1998	011	Labeling Revision	Letter
5/10/1995	010	Manufacturing Change or Addition
11/22/1993	009	Labeling Revision
11/8/1993	008	Control Supplement
10/27/1989	006	Manufacturing Change or Addition
10/31/1988	005	Manufacturing Change or Addition
2/2/1989	004	Control Supplement
8/14/1986	001	Package Change
5/28/1986	000	Approval	Review

Therapeutic Equivalents