Drug History: REGONOL

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:	REGONOL
FDA Application No:	(NDA) 017398
Active Ingredient(s):	PYRIDOSTIGMINE BROMIDE
Company:	SANDOZ

Label History

View the label approved on September 29, 2004 for REGONOL, (NDA) 017398

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
9/21/2004	015	Manufacturing Change or Addition	Letter Label
10/17/2003	014	Manufacturing Change or Addition	Letter
7/12/1999	013	Labeling Revision
3/15/1999	012	Manufacturing Change or Addition
3/4/1997	011	Control Supplement
2/28/1994	010	Manufacturing Change or Addition
10/6/1992	009	Manufacturing Change or Addition
10/5/1990	008	Manufacturing Change or Addition
3/30/1988	007	Control Supplement
2/10/1987	006	Control Supplement
3/5/1999	005	Labeling Revision
5/18/1982	004	Labeling Revision
5/18/1982	003	Manufacturing Change or Addition
11/13/1980	002	Labeling Revision
11/13/1980	001	Control Supplement
8/14/1973	000	Approval

Therapeutic Equivalents