Visitor Monitoring Drug History: ZYLOPRIM
 
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Label and Approval History

Drug Name: ZYLOPRIM
FDA Application No: (NDA) 016084
Active Ingredient(s): ALLOPURINOL
Company: PROMETHEUS LABS
 
Label History
 
Labels are not available on this site for ZYLOPRIM, (NDA) 016084
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/17/2002 041Labeling Revision Letter
Review 
7/11/1991 039Control Supplement  
6/7/1985 038Control Supplement  
2/27/1985 037Control Supplement  
6/1/1983 036Formulation Revision  
12/8/1982 035Labeling Revision  
1/27/1986 034Control Supplement  
6/10/1982 033Package Change  
6/10/1982 032Control Supplement  
12/10/1982 031Package Change  
2/25/1985 030Practioner Draft Labeling  
5/16/1989 029Control Supplement  
2/1/1980 027Package Change  
1/30/1980 023Package Change  
4/6/1977 022Control Supplement  
12/6/1976 021Labeling Revision  
1/16/1976 019Control Supplement  
8/19/1966 000Approval  
 
Therapeutic Equivalents
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