Visitor Monitoring Drug History: K-TAB
 
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: K-TAB
FDA Application No: (NDA) 018279
Active Ingredient(s): POTASSIUM CHLORIDE
Company: ABBOTT
 
Label History
 
Labels are not available on this site for KTAB, (NDA) 018279
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/14/2004 027Labeling Revision Letter 
12/24/2002 025Control Supplement  
10/2/2002 024Control Supplement  
4/16/1998 023Package Change  
10/29/1997 022Control Supplement  
11/21/1996 021Control Supplement  
1/27/1993 020Formulation Revision  
3/26/1990 019Package Change  
11/2/1989 017Package Change  
8/1/1988 016Labeling Revision  
8/1/1988 015Control Supplement  
6/12/1987 014Control Supplement  
6/17/1986 012Control Supplement  
10/7/1986 011Formulation Revision  
1/14/1986 010Formulation Revision  
3/25/1985 009Expiration Date Change  
8/13/1984 008Labeling Revision  
8/1/1984 007Control Supplement  
7/2/1982 006Formulation Revision  
11/10/1982 005Labeling Revision  
4/29/1981 004Manufacturing Change or Addition  
1/16/1981 003Manufacturing Change or Addition  
2/3/1981 002Manufacturing Change or Addition  
2/4/1981 001Package Change  
6/9/1980 000Approval  
 
Therapeutic Equivalents
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