Visitor Monitoring Drug Details: GAVISCON
 
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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
 
 
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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