Drug History: LOTRIMIN AF

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	LOTRIMIN AF
FDA Application No:	(NDA) 020889
Active Ingredient(s):	CLOTRIMAZOLE
Company:	SCHERING PLOUGH

Label History

View the label approved on June 8, 2004 for LOTRIMIN AF, (NDA) 020889

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
1/16/2002	006	Control Supplement
3/7/2001	005	Control Supplement
10/4/1999	004	Control Supplement
8/1/2001	002	Labeling Revision	Label
5/19/1998	001	Control Supplement
10/27/1989	000	Approval

Therapeutic Equivalents