Visitor Monitoring Drug History: CARAFATE
 
Drugs Directory of False Positives 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) 019183
Active Ingredient(s): SUCRALFATE
Company: AXCAN SCANDIPHARM
 
Label History
 
View the label approved on May 1, 2007 for CARAFATE, (NDA) 019183


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 DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/26/2007 011Labeling Revision Letter
Label 
2/10/2006 009Package Change Letter 
2/8/2000 007Control Supplement  
7/16/1997 006Control Supplement  
8/14/1997 004Package Change  
8/21/1995 003Package Change  
7/13/1994 002Labeling Revision  
4/11/1994 001Control Supplement  
12/16/1993 000Approval  
 
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