Visitor Monitoring Drug Details: GLYSET
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: GLYSET
FDA Application No: (NDA) 020682
Active Ingredient(s): MIGLITOL
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: December 18, 1996
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no 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
GLYSET MIGLITOL25MGTABLET; ORAL Prescription No None
GLYSET MIGLITOL50MGTABLET; ORAL Prescription No None
GLYSET MIGLITOL100MGTABLET; ORAL Prescription Yes None


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