Visitor Monitoring Drug History: KLOR-CON
 
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: KLOR-CON
FDA Application No: (NDA) 019123
Active Ingredient(s): POTASSIUM CHLORIDE
Company: UPSHER SMITH
 
Label History
 
Labels are not available on this site for KLORCON, (NDA) 019123
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/13/2006 024Labeling Revision Letter 
5/24/2004 022Labeling Revision Letter 
11/21/2003 021Labeling Revision Letter 
7/18/1996 019Package Change  
7/18/1995 018Control Supplement  
4/8/1994 017Manufacturing Change or Addition  
12/16/1994 016Manufacturing Change or Addition  
7/2/1993 015Package Change  
10/31/1991 014Control Supplement  
7/17/1990 013Formulation Revision  
9/21/1989 012Control Supplement  
7/18/1990 011Control Supplement  
9/18/1989 010Control Supplement  
7/24/1989 009Control Supplement  
6/26/1992 008Comparative Efficacy Claim  
11/7/1988 007Manufacturing Change or Addition  
6/2/1988 006Labeling Revision  
7/31/1987 005Control Supplement  
8/25/1987 004Package Change  
6/26/1987 003Manufacturing Change or Addition  
4/17/1987 002Formulation Revision  
4/17/1986 000Approval  
 
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