Drug History: CARAFATE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	CARAFATE
FDA Application No:	(NDA) 018333
Active Ingredient(s):	SUCRALFATE
Company:	AXCAN SCANDIPHARM

Label History

View the label approved on May 1, 2007 for CARAFATE, (NDA) 018333

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
4/26/2007	032	Labeling Revision	Letter Label
11/29/1995	029	Package Change
8/15/1995	028	Package Change
7/14/1994	027	Labeling Revision
12/28/1992	026	Labeling Revision
2/12/1991	025	Labeling Revision
10/5/1990	024	Control Supplement
5/11/1990	023	Labeling Revision
12/16/1988	022	Package Change
5/5/1988	018	Package Change
12/19/1988	017	Labeling Revision
7/2/1986	014	Labeling Revision
8/5/1987	012	Control Supplement
9/24/1985	011	Package Change
8/5/1987	010	Control Supplement
5/11/1990	009	New or Modified Indication
5/14/1985	008	Labeling Revision
9/24/1984	006	Labeling Revision
4/22/1983	005	Labeling Revision
6/1/1983	004	Package Change
6/9/1983	003	Package Change
8/16/1982	002	Labeling Revision
3/9/1982	001	Package Change
10/30/1981	000	Approval

Therapeutic Equivalents