Drug History: ORAPRED

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:	ORAPRED
FDA Application No:	(ANDA) 075117
Active Ingredient(s):	PREDNISOLONE SODIUM PHOSPHATE
Company:	ASCENT PEDS

Label History

View the label approved on December 14, 2000 for ORAPRED, (ANDA) 075117

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
11/7/2002	006	Control Supplement
5/8/2002	005	Control Supplement
8/28/2001	004	Control Supplement
8/28/2001	003	Facility Addition
6/25/2001	002	Facility Addition
3/28/2001	001	Supplier Addition
12/14/2000	000	Approval	Letter Label Review

Therapeutic Equivalents