Visitor Monitoring Drug History: GLYBURIDE (MICRONIZED)
 
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Label and Approval History

Drug Name: GLYBURIDE (MICRONIZED)
FDA Application No: (ANDA) 074686
Active Ingredient(s): GLYBURIDE
Company: TEVA
 
Label History
 
Labels are not available on this site for GLYBURIDE (MICRONIZED), (ANDA) 074686
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/2/2002 010Control Supplement  
10/2/2002 009Manufacturing Revision  
10/2/2002 008Facility Addition  
7/1/2002 007Facility Addition  
9/13/2000 006Control Supplement  
2/15/2000 005Labeling  
8/28/2000 004Packaging Addition  
8/28/2000 003Labeling  
4/20/1999 000Approval Letter
Review 
11/10/1998 000Tentative Approval Letter
Review 
 
Therapeutic Equivalents
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