Drug History: NEURONTIN

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:	NEURONTIN
FDA Application No:	(NDA) 020882
Active Ingredient(s):	GABAPENTIN
Company:	PFIZER PHARMS

Label History

View the label approved on February 23, 2005 for NEURONTIN, (NDA) 020882

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
5/3/2006	021	Labeling Revision	Letter
4/30/2004	017	Control Supplement	Letter
2/18/2005	015	Labeling Revision	Letter Label
12/19/2002	012	Control Supplement
10/24/2002	010	Manufacturing Change or Addition
8/15/2002	009	Efficacy Supplement with Clinical Data to Support	Letter
1/30/2002	008	Labeling Revision	Letter
1/18/2002	007	Control Supplement
9/19/2000	005	Manufacturing Change or Addition
10/12/2000	002	New or Modified Indication	Letter Label Review
10/9/1998	000	Approval	Letter Review

Therapeutic Equivalents