Visitor Monitoring Drug History: K-DUR 10
 
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Label and Approval History

Drug Name: K-DUR 10
FDA Application No: (NDA) 019439
Active Ingredient(s): POTASSIUM CHLORIDE
Company: KEY PHARMS
 
Label History
 
Labels are not available on this site for KDUR 10, (NDA) 019439
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/21/2001 021Manufacturing Change or Addition  
9/1/2000 020Manufacturing Change or Addition  
3/21/1997 019Manufacturing Change or Addition  
11/15/1996 018Manufacturing Change or Addition  
11/8/1993 017Manufacturing Change or Addition  
12/20/1990 015Labeling Revision  
8/8/1989 014Labeling Revision  
3/15/1989 012Control Supplement  
8/3/1990 011Control Supplement  
4/4/1989 010Manufacturing Change or Addition  
3/15/1989 009Package Change  
10/26/1988 008Manufacturing Change or Addition  
10/4/1988 007Control Supplement  
6/2/1988 005Manufacturing Change or Addition  
5/5/1988 004Control Supplement  
8/23/1988 003Labeling Revision  
8/12/1987 002Labeling Revision  
8/23/1988 001Labeling Revision  
6/13/1986 000Approval  
 
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