Visitor Monitoring Drug History: SLOW-K
 
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: SLOW-K
FDA Application No: (NDA) 017476
Active Ingredient(s): POTASSIUM CHLORIDE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for SLOWK, (NDA) 017476
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/24/2004 045Supplement Letter 
11/24/2004 044Supplement Letter 
4/28/1999 043Package Change  
11/22/1996 041Expiration Date Change  
6/30/1992 040Control Supplement  
5/20/1991 039Control Supplement  
8/8/1989 038Package Change  
3/23/1988 037Labeling Revision  
10/31/1986 036Control Supplement  
8/21/1985 035Control Supplement  
3/19/1985 034Control Supplement  
12/14/1984 033Control Supplement  
5/22/1984 032Control Supplement  
4/6/1983 030Package Change  
10/22/1982 029Package Change  
9/14/1981 028Manufacturing Change or Addition  
9/14/1981 027Formulation Revision  
7/21/1981 026Control Supplement  
6/13/1980 025Control Supplement  
1/21/1980 024Package Change  
7/2/1982 023Formulation Revision  
5/4/1979 022Package Change  
8/3/1979 021Package Change  
8/3/1979 020Package Change  
8/3/1979 019Package Change  
1/3/1980 018Labeling Revision  
7/8/1982 017Package Change  
1/9/1978 016Control Supplement  
6/27/1977 015Labeling Revision  
4/7/1981 014Manufacturing Change or Addition  
6/29/1979 013Package Change  
2/8/1977 012Control Supplement  
2/8/1977 011Manufacturing Change or Addition  
2/8/1977 010Control Supplement  
6/7/1976 009Manufacturing Change or Addition  
6/29/1976 008Manufacturing Change or Addition  
4/1/1976 007Formulation Revision  
4/1/1976 004Control Supplement  
11/18/1975 003Control Supplement  
1/9/1976 002Control Supplement  
8/20/1975 001Control Supplement  
4/25/1975 000Approval  
 
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