Visitor Monitoring Drug Details: GLYBURIDE
 
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Drug Details

Drug Name: GLYBURIDE
FDA Application No: (ANDA) 075947
Active Ingredient(s): GLYBURIDE
Company: ACTAVIS TOTOWA
Original Approval or Tentative Approval Date: November 14, 2002
 
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
GLYBURIDE GLYBURIDE1.5MGTABLET; ORAL Prescription No AB
GLYBURIDE GLYBURIDE3MGTABLET; ORAL Prescription No AB
GLYBURIDE GLYBURIDE6MGTABLET; ORAL Prescription No AB


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