Drug History: LAC-HYDRIN

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:	LAC-HYDRIN
FDA Application No:	(NDA) 020508
Active Ingredient(s):	AMMONIUM LACTATE
Company:	RANBAXY

Label History

View the label approved on December 30, 2004 for LACHYDRIN, (NDA) 020508

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
12/13/2004	006	Labeling Revision	Letter Label
8/25/2000	005	Efficacy Supplement with Clinical Data to Support	Letter Label Review
7/19/1999	004	Package Change
5/13/1998	003	Manufacturing Change or Addition
3/21/1998	002	Formulation Revision
8/29/1996	000	Approval

Therapeutic Equivalents