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) 020888
Active Ingredient(s):	CLOTRIMAZOLE
Company:	SCHERING PLOUGH

Label History

View the label approved on April 24, 2003 for LOTRIMIN AF, (NDA) 020888

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	007	Control Supplement
3/8/2001	006	Control Supplement
2/26/2001	005	Control Supplement
12/9/1998	004	Package Change
8/1/2001	002	Labeling Revision	Label
6/9/1998	001	Control Supplement
10/27/1989	000	Approval

Therapeutic Equivalents