Visitor Monitoring Drug History: KLOTRIX
 
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: KLOTRIX
FDA Application No: (NDA) 017850
Active Ingredient(s): POTASSIUM CHLORIDE
Company: APOTHECON
 
Label History
 
Labels are not available on this site for KLOTRIX, (NDA) 017850
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/3/1995 028Control Supplement  
10/3/1990 027Formulation Revision  
9/19/1989 026Labeling Revision  
6/15/1988 025Control Supplement  
6/7/1988 024Package Change  
8/26/1988 023Labeling Revision  
10/1/1987 022Control Supplement  
5/15/1987 021Package Change  
2/13/1987 020Package Change  
3/11/1987 019Manufacturing Change or Addition  
10/24/1985 018Package Change  
10/24/1985 017Package Change  
5/24/1985 016Package Change  
7/30/1985 015Control Supplement  
5/15/1985 014Package Change  
6/14/1985 013Expiration Date Change  
6/9/1983 012Control Supplement  
6/9/1983 011Control Supplement  
5/4/1983 010Package Change  
5/4/1983 009Control Supplement  
5/4/1983 008Manufacturing Change or Addition  
1/4/1983 007Manufacturing Change or Addition  
2/4/1982 006Control Supplement  
10/1/1981 005Labeling Revision  
8/13/1984 004Practioner Draft Labeling  
3/17/1981 003Control Supplement  
8/14/1980 002Package Change  
8/14/1980 001Package Change  
5/22/1980 000Approval  
 
Therapeutic Equivalents
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