Visitor Monitoring Drug Details: GLIPIZIDE
 
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Drug Details

Drug Name: GLIPIZIDE
FDA Application No: (ANDA) 076467
Active Ingredient(s): GLIPIZIDE
Company: WATSON LABS
Original Approval or Tentative Approval Date: September 8, 2003
 
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
GLIPIZIDE GLIPIZIDE5MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB
GLIPIZIDE GLIPIZIDE10MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB
GLIPIZIDE GLIPIZIDE2.5MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB


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