Drug History: YASMIN

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	YASMIN
FDA Application No:	(NDA) 021098
Active Ingredient(s):	DROSPIRENONE; ETHINYL ESTRADIOL
Company:	BAYER HLTHC

Label History

View the label approved on May 13, 2003 for YASMIN, (NDA) 021098

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
8/8/2002	006	Manufacturing Change or Addition
5/9/2003	005	Efficacy Supplement with Clinical Data to Support	Letter Label
12/12/2001	004	Control Supplement
11/30/2001	003	Manufacturing Change or Addition
11/30/2001	002	Manufacturing Change or Addition
11/26/2001	001	Package Change
5/11/2001	000	Approval	Letter Label Review Consumer Information Sheet

There are no Therapeutic Equivalents