Visitor Monitoring Drug Details: GAVISCON
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: GAVISCON
FDA Application No: (NDA) 018685
Active Ingredient(s): ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: December 9, 1983
Chemical Type: 4 New combination
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
GAVISCON ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE80MG; 20MGTABLET, CHEWABLE; ORAL OTC No None
GAVISCON ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE160MG; 40MGTABLET, CHEWABLE; ORAL OTC Yes None


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