Visitor Monitoring Drug History: RENACIDIN
 
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: RENACIDIN
FDA Application No: (NDA) 019481
Active Ingredient(s): CITRIC ACID; GLUCONOLACTONE; MAGNESIUM CARBONATE
Company: UNITED GUARDIAN
 
Label History
 
Labels are not available on this site for RENACIDIN, (NDA) 019481
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/3/2007 007Manufacturing Change or Addition Letter 
9/30/1998 006Control Supplement  
8/31/1998 005Control Supplement  
10/28/1996 004Control Supplement  
12/3/1993 003Control Supplement  
4/13/1993 002Control Supplement  
4/16/1993 001Manufacturing Change or Addition  
10/2/1990 000Approval  
 
There are no Therapeutic Equivalents
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