Visitor Monitoring Drug History: ALLOPURINOL
 
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Label and Approval History

Drug Name: ALLOPURINOL
FDA Application No: (NDA) 018877
Active Ingredient(s): ALLOPURINOL
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for ALLOPURINOL, (NDA) 018877
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/14/2002 031Control Supplement  
4/25/2001 030Control Supplement  
2/5/2001 029Control Supplement  
3/30/1998 026Chemistry  
3/30/1998 025Chemistry  
7/30/1993 021Chemistry in Effect  
1/28/1991 020Chemistry  
5/31/1991 019Chemistry  
6/29/1990 018Chemistry  
7/7/1988 017Chemistry  
7/7/1988 016Chemistry  
12/17/1987 015Chemistry  
12/17/1987 014Chemistry  
12/17/1987 013Chemistry  
3/11/1987 011Chemistry  
7/3/1985 007Chemistry  
7/3/1985 006Chemistry  
5/10/1985 004Chemistry  
5/10/1985 003Chemistry  
7/3/1985 002Chemistry  
9/28/1984 000Approval  
 
Therapeutic Equivalents
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