Drug History: TYLENOL (CAPLET)

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	TYLENOL (CAPLET)
FDA Application No:	(NDA) 019872
Active Ingredient(s):	ACETAMINOPHEN
Company:	MCNEIL CONS

Label History

View the label approved on June 8, 2003 for TYLENOL (CAPLET), (NDA) 019872

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
11/3/2004	021	Package Change	Letter
4/13/2004	018	Labeling Revision	Letter
3/22/2004	017	Package Change	Letter
8/1/2003	016	Control Supplement	Letter
5/28/2003	014	Labeling Revision	Letter Label
5/28/2003	013	Labeling Revision	Letter Label
5/29/2003	012	Labeling Revision	Letter Label
2/12/2001	011	Manufacturing Change or Addition
7/25/2000	010	Package Change
7/25/2000	009	Labeling Revision
1/11/2001	006	Formulation Revision
8/1/1995	005	Control Supplement
1/5/1995	003	Control Supplement
7/28/1995	002	Package Change
11/23/1994	001	Package Change
6/8/1994	000	Approval

Therapeutic Equivalents