Drug History: NEO TECT KIT

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:	NEO TECT KIT
FDA Application No:	(NDA) 021012
Active Ingredient(s):	TECHNETIUM TC-99M DEPREOTIDE
Company:	CIS BIO INTL SA

Label History

View the label approved on October 8, 2004 for NEO TECT KIT, (NDA) 021012

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
10/1/2004	007	Formulation Revision	Letter Label
1/30/2002	003	Control Supplement
4/11/2001	002	Control Supplement
4/26/2001	001	Manufacturing Change or Addition
8/3/1999	000	Approval	Letter Label Review Consumer Information Sheet

There are no Therapeutic Equivalents