FDA Drug Application (072687) for FOAMICON by NOVARTIS

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Application Number072687
Product Number001
FormTABLET, CHEWABLE;ORAL
Dosage80MG;20MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameFOAMICON
Active IngredientALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE

Active IngredientCount
List of drugs with Active Ingredient ALUMINUM HYDROXIDE4
List of drugs with Active Ingredient MAGNESIUM TRISILICATE4


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