Drug History: ACTOPLUS MET

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	ACTOPLUS MET
FDA Application No:	(NDA) 021842
Active Ingredient(s):	METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
Company:	TAKEDA GLOBAL

Label History

View the label approved on September 26, 2007 for ACTOPLUS MET, (NDA) 021842

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
9/26/2007	005	Labeling Revision	Letter Label
9/28/2006	003	Labeling Revision	Letter
11/4/2006	002	Labeling Revision	Letter Label
8/30/2006	001	Labeling Revision	Letter Label
8/29/2005	000	Approval	Letter Label Review Patient Package Insert

There are no Therapeutic Equivalents