Visitor Monitoring Drug History: GAVISCON
 
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: GAVISCON
FDA Application No: (NDA) 018685
Active Ingredient(s): ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for GAVISCON, (NDA) 018685
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/13/2002 015Control Supplement  
11/8/2000 014Control Supplement  
9/22/2000 013Manufacturing Change or Addition  
2/28/2000 012Manufacturing Change or Addition  
2/7/2000 011Control Supplement  
10/4/1999 010Control Supplement  
3/17/1998 009Control Supplement  
12/1/1997 008Manufacturing Change or Addition  
12/1/1997 007Control Supplement  
4/29/1999 006Package Change  
1/25/1995 005Labeling Revision  
10/1/1991 004Package Change  
2/8/1989 003Package Change  
2/25/1985 002Package Change  
8/1/1984 001Formulation Revision  
12/9/1983 000Approval  
 
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