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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 072687
Company: NOVARTIS

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
FOAMICON ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE 80MG;20MG TABLET, CHEWABLE;ORAL Discontinued None No No
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