Visitor Monitoring Drug History: DIULO
 
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: DIULO
FDA Application No: (NDA) 018535
Active Ingredient(s): METOLAZONE
Company: GD SEARLE LLC
 
Label History
 
Labels are not available on this site for DIULO, (NDA) 018535
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/28/1990 006Labeling Revision  
9/22/1988 005Labeling Revision  
7/24/1986 004Labeling Revision  
1/11/1983 003Labeling Revision  
11/29/1982 002Labeling Revision  
2/24/1981 000Approval  
 
There are no Therapeutic Equivalents
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