Visitor Monitoring Drug Details: GLYBURIDE
 
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Drug Details

Drug Name: GLYBURIDE
FDA Application No: (ANDA) 074388
Active Ingredient(s): GLYBURIDE
Company: TEVA
Original Approval or Tentative Approval Date: August 29, 1995
 
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 GLYBURIDE1.25MGTABLET; ORAL Prescription No AB
GLYBURIDE GLYBURIDE2.5MGTABLET; ORAL Prescription No AB
GLYBURIDE GLYBURIDE5MGTABLET; ORAL Prescription No AB


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