Drug History: CYLERT

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:	CYLERT
FDA Application No:	(NDA) 016832
Active Ingredient(s):	PEMOLINE
Company:	ABBOTT

Label History

View the label approved on October 19, 2005 for CYLERT, (NDA) 016832

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
11/21/2003	022	Labeling Revision	Letter Label
1/6/2003	021	Control Supplement
9/12/2002	020	Control Supplement
9/4/2002	019	Control Supplement
5/28/1999	018	Labeling Revision
5/8/1998	016	Package Change	Review
12/12/1997	015	Labeling Revision	Review
9/9/1996	014	Control Supplement	Review
4/11/1996	013	Labeling Revision	Review
2/16/1990	012	Manufacturing Change or Addition
6/15/1987	011	Labeling Revision
9/6/1984	009	Labeling Revision
3/30/1979	006	Labeling Revision
6/6/1978	005	Package Change
10/12/1977	004	Formulation Revision
3/14/1979	003	Labeling Revision
3/25/1975	001	Control Supplement
1/27/1975	000	Approval

Therapeutic Equivalents