Visitor Monitoring Drug Details: SANOREX
 
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Drug Details

Drug Name: SANOREX
FDA Application No: (NDA) 017247
Active Ingredient(s): MAZINDOL
Company: NOVARTIS
Original Approval or Tentative Approval Date: June 14, 1973
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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
SANOREX MAZINDOL1MGTABLET; ORAL Discontinued No None
SANOREX MAZINDOL2MGTABLET; ORAL Discontinued No None


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