FDA Drug Application (017247) for SANOREX by NOVARTIS

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Application Number017247
Product Number001
FormTABLET;ORAL
Dosage1MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameSANOREX
Active IngredientMAZINDOL

Active IngredientCount
List of drugs with Active Ingredient MAZINDOL2


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