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

Drug Name: GLYBURIDE (MICRONIZED)
FDA Application No: (NDA) 020055
Active Ingredient(s): GLYBURIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for GLYBURIDE (MICRONIZED), (NDA) 020055
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/8/2000 007Manufacturing Change or Addition  
2/5/1999 006Package Change  
12/4/1998 005Package Change  
12/24/1997 004Manufacturing Change or Addition  
5/13/1997 003Control Supplement  
2/1/1995 002Labeling Revision  
2/7/1995 001Control Supplement  
4/17/1992 000Approval  
 
There are no Therapeutic Equivalents
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