Visitor Monitoring Drug History: LOPURIN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: LOPURIN
FDA Application No: (NDA) 018297
Active Ingredient(s): ALLOPURINOL
Company: ABBOTT
 
Label History
 
Labels are not available on this site for LOPURIN, (NDA) 018297
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/21/1986 015Manufacturing Change or Addition  
3/18/1986 014Package Change  
5/31/1985 013Formulation Revision  
11/18/1985 011Package Change  
3/6/1985 010Expiration Date Change  
1/31/1986 009Control Supplement  
3/25/1981 007Expiration Date Change  
2/15/1985 006Formulation Revision  
6/10/1981 004Formulation Revision  
1/11/1982 003Formulation Revision  
1/11/1982 002Formulation Revision  
4/27/1981 001Labeling Revision  
6/10/1980 000Approval  
 
Therapeutic Equivalents
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