Visitor Monitoring Drug History: DARANIDE
 
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: DARANIDE
FDA Application No: (NDA) 011366
Active Ingredient(s): DICHLORPHENAMIDE
Company: MERCK
 
Label History
 
Labels are not available on this site for DARANIDE, (NDA) 011366
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/24/1994 027Labeling Revision  
6/13/1995 026Control Supplement  
6/2/1989 025Manufacturing Change or Addition  
2/12/1991 024Control Supplement  
9/6/1985 023Labeling Revision  
9/6/1985 022Control Supplement  
8/6/1984 021Control Supplement  
2/26/1982 020Control Supplement  
11/5/1986 018Practioner Draft Labeling  
12/18/1979 017Labeling Revision  
12/20/1979 016Labeling Revision  
7/28/1978 015Control Supplement  
7/22/1958 000Approval  
 
There are no Therapeutic Equivalents
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